ICD-10-CM Disease, diseased References
"Disease, diseased" Annotation Back-References in the ICD-10-CM Index to Diseases and Injuries
Browse the ICD-10-CM codes with references applicable to the clinical term "disease, diseased"
- Disease, diseased - See Also: Syndrome;
- absorbent system - I87.8 Other specified disorders of veins
- acid-peptic - K30 Functional dyspepsia
- Acosta's - T70.29 Other effects of high altitude
- Adams-Stokes (-Morgagni) (syncope with heart block) - I45.9 Conduction disorder, unspecified
- Addison's anemia (pernicious) - D51.0 Vitamin B12 deficiency anemia due to intrinsic factor deficiency
- adenoids (and tonsils) - J35.9 Chronic disease of tonsils and adenoids, unspecified
- adrenal (capsule) (cortex) (gland) (medullary) - E27.9 Disorder of adrenal gland, unspecified
- ainhum - L94.6 Ainhum
- airway
- akamushi (scrub typhus) - A75.3 Typhus fever due to Rickettsia tsutsugamushi
- Albers-Schönberg (marble bones) - Q78.2 Osteopetrosis
- Albert's - See: Tendinitis, Achilles;
- Alexander - G31.86 Alexander disease
- alimentary canal - K63.9 Disease of intestine, unspecified
- alligator-skin - Q80.9 Congenital ichthyosis, unspecified
- acquired - L85.0 Acquired ichthyosis
- alpha heavy chain - C88.3 Immunoproliferative small intestinal disease
- alpine - T70.29 Other effects of high altitude
- altitude - T70.20 Unspecified effects of high altitude
- alveolar ridge
- alveoli, teeth - K08.9 Disorder of teeth and supporting structures, unspecified
- Alzheimer's - See Also: Dementia, in, diseases specified elsewhere; - G30.9 Alzheimer's disease, unspecified
- early onset - See Also: Dementia, in, diseases specified elsewhere; - G30.0 Alzheimer's disease with early onset
- with behavioral disturbance - See Also: Dementia, in, diseases specified elsewhere; - G30.0 Alzheimer's disease with early onset
- late onset - See Also: Dementia, in, diseases specified elsewhere; - G30.1 Alzheimer's disease with late onset
- with behavioral disturbance - See Also: Dementia, in, diseases specified elsewhere; - G30.1 Alzheimer's disease with late onset
- specified NEC - See Also: Dementia, in, diseases specified elsewhere; - G30.8 Other Alzheimer's disease
- with behavioral disturbance - See Also: Dementia, in, diseases specified elsewhere; - G30.8 Other Alzheimer's disease
- with behavioral disturbance - See Also: Dementia, in, diseases specified elsewhere; - G30.9 Alzheimer's disease, unspecified
- early onset - See Also: Dementia, in, diseases specified elsewhere; - G30.0 Alzheimer's disease with early onset
- amyloid - See: Amyloidosis;
- Andersen's (glycogenosis IV) - E74.09 Other glycogen storage disease
- Andes - T70.29 Other effects of high altitude
- Andrews' (bacterid) - L08.89 Other specified local infections of the skin and subcutaneous tissue
- angiospastic - I73.9 Peripheral vascular disease, unspecified
- anterior
- antiglomerular basement membrane (anti- GBM) antibody - M31.0 Hypersensitivity angiitis
- tubulo-interstitial nephritis - N12 Tubulo-interstitial nephritis, not specified as acute or chronic
- Antopol - E74.05 Lysosome-associated membrane protein 2 [LAMP2] deficiency
- antral - See: Sinusitis, maxillary;
- anus - K62.9 Disease of anus and rectum, unspecified
- specified NEC - K62.89 Other specified diseases of anus and rectum
- aorta (nonsyphilitic) - I77.9 Disorder of arteries and arterioles, unspecified
- syphilitic NEC - A52.02 Syphilitic aortitis
- aortic (heart) (valve) - I35.9 Nonrheumatic aortic valve disorder, unspecified
- rheumatic - I06.9 Rheumatic aortic valve disease, unspecified
- Apollo - B30.3 Acute epidemic hemorrhagic conjunctivitis (enteroviral)
- aponeuroses - See: Enthesopathy;
- appendix - K38.9 Disease of appendix, unspecified
- specified NEC - K38.8 Other specified diseases of appendix
- aqueous (chamber) - H21.9 Unspecified disorder of iris and ciliary body
- Arnold-Chiari - See: Arnold-Chiari disease;
- arterial - See Also: Disease, artery; - I77.9 Disorder of arteries and arterioles, unspecified
- arteriocardiorenal - See: Hypertension, cardiorenal;
- arteriolar (generalized) (obliterative) - I77.9 Disorder of arteries and arterioles, unspecified
- arteriorenal - See: Hypertension, kidney;
- arteriosclerotic - See Also: Arteriosclerosis;
- cardiovascular - See: Disease, heart, ischemic, atherosclerotic;
- coronary (artery) - See: Disease, heart, ischemic, atherosclerotic;
- heart - See: Disease, heart, ischemic, atherosclerotic;
- artery - See Also: Disease, arterial; - I77.9 Disorder of arteries and arterioles, unspecified
- atticoantral, chronic - H66.20 Chronic atticoantral suppurative otitis media, unspecified ear
- auditory canal - See: Disorder, ear, external;
- auricle, ear NEC - See: Disorder, pinna;
- Australian X - A83.4 Australian encephalitis
- autoimmune (systemic) NOS - M35.9 Systemic involvement of connective tissue, unspecified
- hemolytic - D59.10 Autoimmune hemolytic anemia, unspecified
- cold type (primary) (secondary) (symptomatic) - D59.12 Cold autoimmune hemolytic anemia
- drug-induced - D59.0 Drug-induced autoimmune hemolytic anemia
- mixed type (primary) (secondary) (symptomatic) - D59.13 Mixed type autoimmune hemolytic anemia
- warm type (primary) (secondary) (symptomatic) - D59.11 Warm autoimmune hemolytic anemia
- thyroid - E06.3 Autoimmune thyroiditis
- hemolytic - D59.10 Autoimmune hemolytic anemia, unspecified
- autoinflammatory - M04.9 Autoinflammatory syndrome, unspecified
- aviator's - See: Effect, adverse, high altitude;
- Ayerza's (pulmonary artery sclerosis with pulmonary hypertension) - I27.0 Primary pulmonary hypertension
- Babington's (familial hemorrhagic telangiectasia) - I78.0 Hereditary hemorrhagic telangiectasia
- bacterial - A49.9 Bacterial infection, unspecified
- Baelz's (cheilitis glandularis apostematosa) - K13.0 Diseases of lips
- bagasse - J67.1 Bagassosis
- balloon - See: Effect, adverse, high altitude;
- Bang's (brucella abortus) - A23.1 Brucellosis due to Brucella abortus
- Bannister's - T78.3 Angioneurotic edema
- barometer makers' - See: Poisoning, mercury;
- Barraquer (-Simons') (progressive lipodystrophy) - E88.1 Lipodystrophy, not elsewhere classified
- Barrett's - See: Barrett's, esophagus;
- Bartholin's gland - N75.9 Disease of Bartholin's gland, unspecified
- basal ganglia - G25.9 Extrapyramidal and movement disorder, unspecified
- Basedow's (exophthalmic goiter) - See: Hyperthyroidism, with, goiter (diffuse);
- Bateman's - B08.1 Molluscum contagiosum
- Batten-Steinert - G71.11 Myotonic muscular dystrophy
- Battey - A31.0 Pulmonary mycobacterial infection
- Beard's (neurasthenia) - F48.8 Other specified nonpsychotic mental disorders
- Becker
- Begbie's (exophthalmic goiter) - See: Hyperthyroidism, with, goiter (diffuse);
- behavioral, organic - F07.9 Unspecified personality and behavioral disorder due to known physiological condition
- Beigel's (white piedra) - B36.2 White piedra
- Benson's - See: Deposit, crystalline;
- Bernard-Soulier (thrombopathy) - D69.1 Qualitative platelet defects
- Bernhardt (-Roth) - See: Mononeuropathy, lower limb, meralgia paresthetica;
- Biermer's (pernicious anemia) - D51.0 Vitamin B12 deficiency anemia due to intrinsic factor deficiency
- bile duct (common) (hepatic) - K83.9 Disease of biliary tract, unspecified
- specified NEC - K83.8 Other specified diseases of biliary tract
- with calculus, stones - See: Calculus, bile duct;
- biliary (tract) - K83.9 Disease of biliary tract, unspecified
- specified NEC - K83.8 Other specified diseases of biliary tract
- Billroth's - See: Spina bifida;
- bird fancier's - J67.2 Bird fancier's lung
- black lung - J60 Coalworker's pneumoconiosis
- bladder - N32.9 Bladder disorder, unspecified
- bleeder's - D66 Hereditary factor VIII deficiency
- blood - D75.9 Disease of blood and blood-forming organs, unspecified
- Bloodgood's - See: Mastopathy, cystic;
- Blount - M92.51 Juvenile osteochondrosis of proximal tibia
- Bodechtel-Guttmann (subacute sclerosing panencephalitis) - A81.1 Subacute sclerosing panencephalitis
- bone - See Also: Disorder, bone;
- bone-marrow - D75.9 Disease of blood and blood-forming organs, unspecified
- Borna - A83.9 Mosquito-borne viral encephalitis, unspecified
- Bornholm (epidemic pleurodynia) - B33.0 Epidemic myalgia
- Bouchard's (myopathic dilatation of the stomach) - K31.0 Acute dilatation of stomach
- Bouillaud's (rheumatic heart disease) - I01.9 Acute rheumatic heart disease, unspecified
- Bourneville (-Brissaud) (tuberous sclerosis) - Q85.1 Tuberous sclerosis
- Bouveret (-Hoffmann) (paroxysmal tachycardia) - I47.9 Paroxysmal tachycardia, unspecified
- bowel - K63.9 Disease of intestine, unspecified
- brain - G93.9 Disorder of brain, unspecified
- arterial, artery - I67.9 Cerebrovascular disease, unspecified
- arteriosclerotic - I67.2 Cerebral atherosclerosis
- congenital - Q04.9 Congenital malformation of brain, unspecified
- degenerative - See: Degeneration, brain;
- inflammatory - See: Encephalitis;
- organic - G93.9 Disorder of brain, unspecified
- arteriosclerotic - I67.2 Cerebral atherosclerosis
- parasitic NEC - B71.9 Cestode infection, unspecified
- senile NEC - G31.1 Senile degeneration of brain, not elsewhere classified
- specified NEC - G93.89 Other specified disorders of brain
- breast - See Also: Disorder, breast; - N64.9 Disorder of breast, unspecified
- cystic (chronic) - See: Mastopathy, cystic;
- fibrocystic - See: Mastopathy, cystic;
- Paget's
- specified NEC - N64.89 Other specified disorders of breast
- Breda's - See: Yaws;
- Bretonneau's (diphtheritic malignant angina) - A36.0 Pharyngeal diphtheria
- Bright's - See: Nephritis;
- arteriosclerotic - See: Hypertension, kidney;
- Brill's (recrudescent typhus) - A75.1 Recrudescent typhus [Brill's disease]
- Brill-Zinsser (recrudescent typhus) - A75.1 Recrudescent typhus [Brill's disease]
- Brion-Kayser - See: Fever, paratyphoid;
- broad
- Brocq-Duhring (dermatitis herpetiformis) - L13.0 Dermatitis herpetiformis
- Brocq's
- bronchopulmonary - J98.4 Other disorders of lung
- bronchus NEC - J98.09 Other diseases of bronchus, not elsewhere classified
- bronze Addison's - E27.1 Primary adrenocortical insufficiency
- tuberculous - A18.7 Tuberculosis of adrenal glands
- budgerigar fancier's - J67.2 Bird fancier's lung
- Buerger's (thromboangiitis obliterans) - I73.1 Thromboangiitis obliterans [Buerger's disease]
- bullous - L13.9 Bullous disorder, unspecified
- Bürger-Grütz (essential familial hyperlipemia) - E78.3 Hyperchylomicronemia
- bursa - See: Bursopathy;
- caisson - T70.3 Caisson disease [decompression sickness]
- California - See: Coccidioidomycosis;
- capillaries - I78.9 Disease of capillaries, unspecified
- specified NEC - I78.8 Other diseases of capillaries
- Carapata - A68.0 Louse-borne relapsing fever
- carcinoid - E34.00 Carcinoid syndrome, unspecified
- cardiac - See: Disease, heart;
- cardiopulmonary, chronic - I27.9 Pulmonary heart disease, unspecified
- cardiorenal (hepatic) (hypertensive) (vascular) - See: Hypertension, cardiorenal;
- cardiovascular (atherosclerotic) - I25.10 Atherosclerotic heart disease of native coronary artery without angina pectoris
- congenital - Q28.9 Congenital malformation of circulatory system, unspecified
- hypertensive - See: Hypertension, heart;
- newborn - P29.9 Cardiovascular disorder originating in the perinatal period, unspecified
- specified NEC - P29.89 Other cardiovascular disorders originating in the perinatal period
- renal (hypertensive) - See: Hypertension, cardiorenal;
- syphilitic (asymptomatic) - A52.00 Cardiovascular syphilis, unspecified
- with angina pectoris - See: Arteriosclerosis, coronary (artery),;
- cartilage - See: Disorder, cartilage;
- Castellani's - A69.8 Other specified spirochetal infections
- Castleman (unicentric) (multicentric) - D47.Z2 Castleman disease
- HHV-8-associated - See Also: Herpesvirus, human, 8; - D47.Z2 Castleman disease
- cat-scratch - A28.1 Cat-scratch disease
- Cavare's (familial periodic paralysis) - G72.3 Periodic paralysis
- cecum - K63.9 Disease of intestine, unspecified
- celiac (adult) (infantile) (with steatorrhea) - K90.0 Celiac disease
- cellular tissue - L98.9 Disorder of the skin and subcutaneous tissue, unspecified
- central core - G71.29 Other congenital myopathy
- cerebellar, cerebellum - See: Disease, brain;
- cerebral - See Also: Disease, brain;
- degenerative - See: Degeneration, brain;
- cerebrospinal - G96.9 Disorder of central nervous system, unspecified
- cerebrovascular - I67.9 Cerebrovascular disease, unspecified
- cervix (uteri) (noninflammatory) - N88.9 Noninflammatory disorder of cervix uteri, unspecified
- inflammatory - See: Cervicitis;
- specified NEC - N88.8 Other specified noninflammatory disorders of cervix uteri
- Chabert's - A22.9 Anthrax, unspecified
- Chandler's (osteochondritis dissecans, hip) - See: Osteochondritis, dissecans, hip;
- Charlouis - See: Yaws;
- Chédiak-Steinbrinck (-Higashi) (congenital gigantism of peroxidase granules) - E70.330 Chediak-Higashi syndrome
- chest - J98.9 Respiratory disorder, unspecified
- Chiari's (hepatic vein thrombosis) - I82.0 Budd-Chiari syndrome
- Chicago - B40.9 Blastomycosis, unspecified
- Chignon - B36.8 Other specified superficial mycoses
- chigo, chigoe - B88.1 Tungiasis [sandflea infestation]
- childhood granulomatous - D71 Functional disorders of polymorphonuclear neutrophils
- Chinese liver fluke - B66.1 Clonorchiasis
- chlamydial - A74.9 Chlamydial infection, unspecified
- specified NEC - A74.89 Other chlamydial diseases
- cholecystic - K82.9 Disease of gallbladder, unspecified
- choroid - H31.9 Unspecified disorder of choroid
- specified NEC - H31.8 Other specified disorders of choroid
- Christmas - D67 Hereditary factor IX deficiency
- chronic bullous of childhood - L12.2 Chronic bullous disease of childhood
- chylomicron retention - E78.3 Hyperchylomicronemia
- ciliary body - H21.9 Unspecified disorder of iris and ciliary body
- specified NEC - H21.89 Other specified disorders of iris and ciliary body
- circulatory (system) NEC - I99.8 Other disorder of circulatory system
- coagulation factor deficiency (congenital) - See: Defect, coagulation;
- coccidioidal - See: Coccidioidomycosis;
- cold
- collagen NOS (nonvascular) (vascular) - M35.9 Systemic involvement of connective tissue, unspecified
- specified NEC - M35.89 Other specified systemic involvement of connective tissue
- colon - K63.9 Disease of intestine, unspecified
- colonic inflammatory bowel, unclassified (IBDU) - K52.3 Indeterminate colitis
- combined system - See: Degeneration, combined;
- compressed air - T70.3 Caisson disease [decompression sickness]
- Concato's (pericardial polyserositis) - A19.9 Miliary tuberculosis, unspecified
- nontubercular - I31.1 Chronic constrictive pericarditis
- pleural - See: Pleurisy, with effusion;
- conjunctiva - H11.9 Unspecified disorder of conjunctiva
- connective tissue, systemic (diffuse) - M35.9 Systemic involvement of connective tissue, unspecified
- Conor and Bruch's (boutonneuse fever) - A77.1 Spotted fever due to Rickettsia conorii
- Cooper's - See: Mastopathy, cystic;
- Cori's (glycogenosis III) - E74.03 Cori disease
- corkhandler's or corkworker's - J67.3 Suberosis
- cornea - H18.9 Unspecified disorder of cornea
- specified NEC - H18.89 Other specified disorders of cornea
- coronary (artery) - See: Disease, heart, ischemic, atherosclerotic;
- corpus cavernosum - N48.9 Disorder of penis, unspecified
- specified NEC - N48.89 Other specified disorders of penis
- Cotugno - See: Sciatica;
- COVID-19 - U07.1 COVID-19
- coxsackie (virus) NEC - B34.1 Enterovirus infection, unspecified
- cranial nerve NOS - G52.9 Cranial nerve disorder, unspecified
- Creutzfeldt-Jakob - See: Creutzfeldt-Jakob disease or syndrome;
- Crocq's (acrocyanosis) - I73.89 Other specified peripheral vascular diseases
- Crohn's - See: Enteritis, regional;
- Curschmann - G71.11 Myotonic muscular dystrophy
- cystic
- cytomegalic inclusion (generalized) - B25.9 Cytomegaloviral disease, unspecified
- Czerny's (periodic hydrarthrosis of the knee) - See: Effusion, joint, knee;
- Daae (-Finsen) (epidemic pleurodynia) - B33.0 Epidemic myalgia
- Danon - E74.05 Lysosome-associated membrane protein 2 [LAMP2] deficiency
- Darling's - See: Histoplasmosis capsulati;
- de Quervain's (tendon sheath) - M65.4 Radial styloid tenosynovitis [de Quervain]
- thyroid (subacute granulomatous thyroiditis) - E06.1 Subacute thyroiditis
- Débove's (splenomegaly) - R16.1 Splenomegaly, not elsewhere classified
- deer fly - See: Tularemia;
- Degos' - I77.89 Other specified disorders of arteries and arterioles
- demyelinating, demyelinizating (nervous system) - G37.9 Demyelinating disease of central nervous system, unspecified
- dense deposit - See Also: N00-N07 with fourth character .6; - N05.6 Unspecified nephritic syndrome with dense deposit disease
- deposition, hydroxyapatite - See: Disease, hydroxyapatite deposition;
- Devergie's (pityriasis rubra pilaris) - L44.0 Pityriasis rubra pilaris
- Devic's - G36.0 Neuromyelitis optica [Devic]
- diaphorase deficiency - D74.0 Congenital methemoglobinemia
- diaphragm - J98.6 Disorders of diaphragm
- diarrheal, infectious NEC - A09 Infectious gastroenteritis and colitis, unspecified
- digestive system - K92.9 Disease of digestive system, unspecified
- specified NEC - K92.89 Other specified diseases of the digestive system
- disc, degenerative - See: Degeneration, intervertebral disc;
- discogenic - See Also: Displacement, intervertebral disc NEC;
- with myelopathy - See: Disorder, disc, with, myelopathy;
- diverticular - See: Diverticula;
- Dubois (thymus) - A50.59 Other late congenital syphilis, symptomatic
- Duchenne-Griesinger - G71.01 Duchenne or Becker muscular dystrophy
- Duchenne's
- ductless glands - E34.9 Endocrine disorder, unspecified
- Duhring's (dermatitis herpetiformis) - L13.0 Dermatitis herpetiformis
- duodenum - K31.9 Disease of stomach and duodenum, unspecified
- specified NEC - K31.89 Other diseases of stomach and duodenum
- Dupré's (meningism) - R29.1 Meningismus
- Dupuytren's (muscle contracture) - M72.0 Palmar fascial fibromatosis [Dupuytren]
- Durand-Nicholas-Favre (climatic bubo) - A55 Chlamydial lymphogranuloma (venereum)
- Duroziez's (congenital mitral stenosis) - Q23.2 Congenital mitral stenosis
- ear - See: Disorder, ear;
- Eberth's - See: Fever, typhoid;
- Ebola (virus) - A98.4 Ebola virus disease
- Ebstein's heart - Q22.5 Ebstein's anomaly
- Echinococcus - See: Echinococcus;
- echovirus NEC - B34.1 Enterovirus infection, unspecified
- Eddowes' (brittle bones and blue sclera) - Q78.0 Osteogenesis imperfecta
- edentulous (alveolar) ridge - K06.9 Disorder of gingiva and edentulous alveolar ridge, unspecified
- specified NEC - K06.8 Other specified disorders of gingiva and edentulous alveolar ridge
- Edsall's - T67.2 Heat cramp
- Eichstedt's (pityriasis versicolor) - B36.0 Pityriasis versicolor
- Eisenmenger's (irreversible) - I27.83 Eisenmenger's syndrome
- Ellis-van Creveld (chondroectodermal dysplasia) - Q77.6 Chondroectodermal dysplasia
- end stage renal (ESRD) - N18.6 End stage renal disease
- due to hypertension - I12.0 Hypertensive chronic kidney disease with stage 5 chronic kidney disease or end stage renal disease
- endocrine glands or system NEC - E34.9 Endocrine disorder, unspecified
- endomyocardial (eosinophilic) - I42.3 Endomyocardial (eosinophilic) disease
- English (rickets) - E55.0 Rickets, active
- epidemic - B99.9 Unspecified infectious disease
- specified NEC - B99.8 Other infectious disease
- epididymis - N50.9 Disorder of male genital organs, unspecified
- Erb (-Landouzy) - G71.02 Facioscapulohumeral muscular dystrophy
- Erdheim-Chester (ECD) - E88.89 Other specified metabolic disorders
- esophagus - K22.9 Disease of esophagus, unspecified
- Eulenburg's (congenital paramyotonia) - G71.19 Other specified myotonic disorders
- eustachian tube - See: Disorder, eustachian tube;
- external
- auditory canal - See: Disorder, ear, external;
- ear - See: Disorder, ear, external;
- extrapyramidal - G25.9 Extrapyramidal and movement disorder, unspecified
- specified NEC - G25.89 Other specified extrapyramidal and movement disorders
- eye - H57.9 Unspecified disorder of eye and adnexa
- eyeball - H44.9 Unspecified disorder of globe
- specified NEC - H44.89 Other disorders of globe
- eyelid - See: Disorder, eyelid;
- specified NEC - See: Disorder, eyelid, specified type NEC;
- eyeworm of Africa - B74.3 Loiasis
- facial nerve (seventh) - G51.9 Disorder of facial nerve, unspecified
- newborn (birth injury) - P11.3 Birth injury to facial nerve
- Fahr (of brain) - G23.8 Other specified degenerative diseases of basal ganglia
- Fahr Volhard (of kidney) - I12.
- fallopian tube (noninflammatory) - N83.9 Noninflammatory disorder of ovary, fallopian tube and broad ligament, unspecified
- inflammatory - See: Salpingo-oophoritis;
- specified NEC - N83.8 Other noninflammatory disorders of ovary, fallopian tube and broad ligament
- familial periodic paralysis - G72.3 Periodic paralysis
- Fanconi ('s) - D61.03 Fanconi anemia
- fascia NEC - See Also: Disorder, muscle;
- inflammatory - See: Myositis;
- specified NEC - M62.89 Other specified disorders of muscle
- Fauchard's (periodontitis) - See: Periodontitis;
- Favre-Durand-Nicolas (climatic bubo) - A55 Chlamydial lymphogranuloma (venereum)
- Fede's - K14.0 Glossitis
- Feer's - See: Poisoning, mercury;
- female pelvic inflammatory - See Also: Disease, pelvis, inflammatory; - N73.9 Female pelvic inflammatory disease, unspecified
- Fernels' (aortic aneurysm) - I71.9 Aortic aneurysm of unspecified site, without rupture
- fibrocaseous of lung - See: Tuberculosis, pulmonary;
- fibrocystic - See: Fibrocystic disease;
- Fiedler's (leptospiral jaundice) - A27.0 Leptospirosis icterohemorrhagica
- fifth - B08.3 Erythema infectiosum [fifth disease]
- file-cutter's - See: Poisoning, lead;
- fish-skin - Q80.9 Congenital ichthyosis, unspecified
- acquired - L85.0 Acquired ichthyosis
- Flajani (-Basedow) (exophthalmic goiter) - See: Hyperthyroidism, with, goiter (diffuse);
- flax-dresser's - J66.1 Flax-dressers' disease
- fluke - See: Infestation, fluke;
- foot and mouth - B08.8 Other specified viral infections characterized by skin and mucous membrane lesions
- foot process - N04.9 Nephrotic syndrome with unspecified morphologic changes
- Forbes' (glycogenosis III) - E74.03 Cori disease
- Fordyce-Fox (apocrine miliaria) - L75.2 Apocrine miliaria
- Fordyce's (ectopic sebaceous glands) (mouth) - Q38.6 Other congenital malformations of mouth
- Forestier's (rhizomelic pseudopolyarthritis) - M35.3 Polymyalgia rheumatica
- meaning ankylosing hyperostosis - See: Hyperostosis, ankylosing;
- Fothergill's
- neuralgia - See: Neuralgia, trigeminal;
- scarlatina anginosa - A38.9 Scarlet fever, uncomplicated
- Fournier (gangrene) - N49.3 Fournier gangrene
- fourth - B08.8 Other specified viral infections characterized by skin and mucous membrane lesions
- Fox (-Fordyce) (apocrine miliaria) - L75.2 Apocrine miliaria
- Francis' - See: Tularemia;
- Franklin - C88.2 Heavy chain disease
- Frei's (climatic bubo) - A55 Chlamydial lymphogranuloma (venereum)
- Friedreich's
- frontal sinus - See: Sinusitis, frontal;
- fungus NEC - B49 Unspecified mycosis
- Gaisböck's (polycythemia hypertonica) - D75.1 Secondary polycythemia
- gallbladder - K82.9 Disease of gallbladder, unspecified
- calculus - See: Calculus, gallbladder;
- cholecystitis - See: Cholecystitis;
- cholesterolosis - K82.4 Cholesterolosis of gallbladder
- fistula - See: Fistula, gallbladder;
- hydrops - K82.1 Hydrops of gallbladder
- obstruction - See: Obstruction, gallbladder;
- perforation - K82.2 Perforation of gallbladder
- specified NEC - K82.8 Other specified diseases of gallbladder
- gamma heavy chain - C88.2 Heavy chain disease
- Gamna's (siderotic splenomegaly) - D73.2 Chronic congestive splenomegaly
- Gamstorp's (adynamia episodica hereditaria) - G72.3 Periodic paralysis
- Gandy-Nanta (siderotic splenomegaly) - D73.2 Chronic congestive splenomegaly
- ganister - J62.8 Pneumoconiosis due to other dust containing silica
- gastric - See: Disease, stomach;
- gastroesophageal reflux (GERD) - K21.9 Gastro-esophageal reflux disease without esophagitis
- gastrointestinal (tract) - K92.9 Disease of digestive system, unspecified
- Gee (-Herter) (-Heubner) (-Thaysen) (nontropical sprue) - K90.0 Celiac disease
- genital organs
- Gerhardt's (erythromelalgia) - I73.81 Erythromelalgia
- Gibert's (pityriasis rosea) - L42 Pityriasis rosea
- Gierke's (glycogenosis I) - E74.01 von Gierke disease
- Gilles de la Tourette's (motor-verbal tic) - F95.2 Tourette's disorder
- gingiva - K06.9 Disorder of gingiva and edentulous alveolar ridge, unspecified
- gland (lymph) - I89.9 Noninfective disorder of lymphatic vessels and lymph nodes, unspecified
- Glanzmann's (hereditary hemorrhagic thrombasthenia) - D69.1 Qualitative platelet defects
- glass-blower's (cataract) - See: Cataract, specified NEC;
- salivary gland hypertrophy - K11.1 Hypertrophy of salivary gland
- Glisson's - See: Rickets;
- globe - H44.9 Unspecified disorder of globe
- specified NEC - H44.89 Other disorders of globe
- glomerular - See Also: Glomerulonephritis;
- glycogen storage - E74.00 Glycogen storage disease, unspecified
- Andersen's - E74.09 Other glycogen storage disease
- Cori's - E74.03 Cori disease
- Forbes' - E74.03 Cori disease
- generalized - E74.00 Glycogen storage disease, unspecified
- glucose-6-phosphatase deficiency - E74.01 von Gierke disease
- heart - E74.02 Pompe disease
- hepatorenal - E74.09 Other glycogen storage disease
- Hers' - E74.09 Other glycogen storage disease
- liver and kidney - E74.09 Other glycogen storage disease
- lysosomal - E74.02 Pompe disease
- McArdle's - E74.04 McArdle disease
- muscle phosphofructokinase - E74.09 Other glycogen storage disease
- myocardium - E74.02 Pompe disease
- Pompe's - E74.02 Pompe disease
- Tauri's - E74.09 Other glycogen storage disease
- type 0 - E74.09 Other glycogen storage disease
- type I - E74.01 von Gierke disease
- type II - E74.02 Pompe disease
- type IIB - E74.05 Lysosome-associated membrane protein 2 [LAMP2] deficiency
- type III - E74.03 Cori disease
- type IV - E74.09 Other glycogen storage disease
- type V - E74.04 McArdle disease
- type VI-XI - E74.09 Other glycogen storage disease
- Von Gierke's - E74.01 von Gierke disease
- Goldstein's (familial hemorrhagic telangiectasia) - I78.0 Hereditary hemorrhagic telangiectasia
- gonococcal NOS - A54.9 Gonococcal infection, unspecified
- graft-versus-host (GVH) - D89.813 Graft-versus-host disease, unspecified
- grainhandler's - J67.8 Hypersensitivity pneumonitis due to other organic dusts
- granulomatous (childhood) (chronic) - D71 Functional disorders of polymorphonuclear neutrophils
- Graves' (exophthalmic goiter) - See: Hyperthyroidism, with, goiter (diffuse);
- Griesinger's - See: Ancylostomiasis;
- Grisel's - M43.6 Torticollis
- Gruby's (tinea tonsurans) - B35.0 Tinea barbae and tinea capitis
- Guillain-Barré - G61.0 Guillain-Barre syndrome
- Guinon's (motor-verbal tic) - F95.2 Tourette's disorder
- gum - K06.9 Disorder of gingiva and edentulous alveolar ridge, unspecified
- gynecological - N94.9 Unspecified condition associated with female genital organs and menstrual cycle
- H (Hartnup's) - E72.02 Hartnup's disease
- Haff - See: Poisoning, mercury;
- Hageman (congenital factor XII deficiency) - D68.2 Hereditary deficiency of other clotting factors
- hair (color) (shaft) - L67.9 Hair color and hair shaft abnormality, unspecified
- Hamman's (spontaneous mediastinal emphysema) - J98.2 Interstitial emphysema
- hand, foot and mouth - B08.4 Enteroviral vesicular stomatitis with exanthem
- Hansen's - See: Leprosy;
- Hantavirus, with pulmonary manifestations - B33.4 Hantavirus (cardio)-pulmonary syndrome [HPS] [HCPS]
- with renal manifestations - A98.5 Hemorrhagic fever with renal syndrome
- Harada's - H30.81 Harada's disease
- Hartnup (pellagra-cerebellar ataxia-renal aminoaciduria) - E72.02 Hartnup's disease
- Hart's (pellagra-cerebellar ataxia-renal aminoaciduria) - E72.02 Hartnup's disease
- Hashimoto's (struma lymphomatosa) - E06.3 Autoimmune thyroiditis
- Hb - See: Disease, hemoglobin;
- heart (organic) - I51.9 Heart disease, unspecified
- amyloid - E85.4 Organ-limited amyloidosis
- aortic (valve) - I35.9 Nonrheumatic aortic valve disorder, unspecified
- arteriosclerotic or sclerotic (senile) - See: Disease, heart, ischemic, atherosclerotic;
- artery, arterial - See: Disease, heart, ischemic, atherosclerotic;
- beer drinkers' - I42.6 Alcoholic cardiomyopathy
- beriberi (wet) - E51.12 Wet beriberi
- black - I27.0 Primary pulmonary hypertension
- congenital - Q24.9 Congenital malformation of heart, unspecified
- coronary - See: Disease, heart, ischemic;
- cryptogenic - I51.9 Heart disease, unspecified
- fibroid - See: Myocarditis;
- functional - I51.89 Other ill-defined heart diseases
- psychogenic - F45.8 Other somatoform disorders
- glycogen storage - E74.02 Pompe disease
- gonococcal - A54.83 Gonococcal heart infection
- hypertensive - See: Hypertension, heart;
- hyperthyroid - See Also: Hyperthyroidism; - E05.90 Thyrotoxicosis, unspecified without thyrotoxic crisis or storm
- with thyroid storm - E05.91 Thyrotoxicosis, unspecified with thyrotoxic crisis or storm
- ischemic (chronic or with a stated duration of over 4 weeks) - I25.9 Chronic ischemic heart disease, unspecified
- atherosclerotic (of) - I25.10 Atherosclerotic heart disease of native coronary artery without angina pectoris
- coronary artery bypass graft - See: Arteriosclerosis, coronary (artery),;
- with angina pectoris - See: Arteriosclerosis, coronary (artery);
- cardiomyopathy - I25.5 Ischemic cardiomyopathy
- diagnosed on ECG or other special investigation, but currently presenting no symptoms - I25.6 Silent myocardial ischemia
- silent - I25.6 Silent myocardial ischemia
- specified form NEC
- atherosclerotic (of) - I25.10 Atherosclerotic heart disease of native coronary artery without angina pectoris
- kyphoscoliotic - I27.1 Kyphoscoliotic heart disease
- meningococcal - A39.50 Meningococcal carditis, unspecified
- mitral - I05.9 Rheumatic mitral valve disease, unspecified
- specified NEC - I05.8 Other rheumatic mitral valve diseases
- muscular - See: Degeneration, myocardial;
- psychogenic (functional) - F45.8 Other somatoform disorders
- pulmonary (chronic) - I27.9 Pulmonary heart disease, unspecified
- rheumatic (chronic) (inactive) (old) (quiescent) (with chorea) - I09.9 Rheumatic heart disease, unspecified
- senile - See: Myocarditis;
- syphilitic - A52.06 Other syphilitic heart involvement
- thyrotoxic - See Also: Thyrotoxicosis; - E05.90 Thyrotoxicosis, unspecified without thyrotoxic crisis or storm
- with thyroid storm - E05.91 Thyrotoxicosis, unspecified with thyrotoxic crisis or storm
- valve, valvular (obstructive) (regurgitant) - See Also: Endocarditis;
- vascular - See: Disease, cardiovascular;
- with
- pulmonary edema (acute) - See Also: Failure, ventricular, left; - I50.1 Left ventricular failure, unspecified
- rheumatic fever (conditions in I00)
- heavy chain NEC - C88.2 Heavy chain disease
- Hebra's
- hematopoietic organs - D75.9 Disease of blood and blood-forming organs, unspecified
- hemoglobin or Hb
- abnormal (mixed) NEC - D58.2 Other hemoglobinopathies
- with thalassemia - D56.9 Thalassemia, unspecified
- AS genotype - D57.3 Sickle-cell trait
- Bart's - D56.0 Alpha thalassemia
- C (Hb-C) - D58.2 Other hemoglobinopathies
- Constant Spring - D58.2 Other hemoglobinopathies
- D (Hb-D) - D58.2 Other hemoglobinopathies
- E (Hb-E) - D58.2 Other hemoglobinopathies
- E-beta thalassemia - D56.5 Hemoglobin E-beta thalassemia
- elliptocytosis - D58.1 Hereditary elliptocytosis
- H (Hb-H) (thalassemia) - D56.0 Alpha thalassemia
- I thalassemia - D56.9 Thalassemia, unspecified
- M - D74.0 Congenital methemoglobinemia
- S or SS - D57.1 Sickle-cell disease without crisis
- beta plus - D57.44 Sickle-cell thalassemia beta plus without crisis
- with
- acute chest syndrome - D57.451 Sickle-cell thalassemia beta plus with acute chest syndrome
- cerebral vascular involvement - D57.453 Sickle-cell thalassemia beta plus with cerebral vascular involvement
- crisis - D57.459 Sickle-cell thalassemia beta plus with crisis, unspecified
- with specified complication NEC - D57.458 Sickle-cell thalassemia beta plus with crisis with other specified complication
- pain (vaso-occlusive) - D57.459 Sickle-cell thalassemia beta plus with crisis, unspecified
- splenic sequestration - D57.452 Sickle-cell thalassemia beta plus with splenic sequestration
- without crisis - D57.44 Sickle-cell thalassemia beta plus without crisis
- with
- beta zero - D57.42 Sickle-cell thalassemia beta zero without crisis
- with
- acute chest syndrome - D57.431 Sickle-cell thalassemia beta zero with acute chest syndrome
- cerebral vascular involvement - D57.433 Sickle-cell thalassemia beta zero with cerebral vascular involvement
- crisis - D57.439 Sickle-cell thalassemia beta zero with crisis, unspecified
- with specified complication NEC - D57.438 Sickle-cell thalassemia beta zero with crisis with other specified complication
- pain (vaso-occlusive) - D57.439 Sickle-cell thalassemia beta zero with crisis, unspecified
- splenic sequestration - D57.432 Sickle-cell thalassemia beta zero with splenic sequestration
- without crisis - D57.42 Sickle-cell thalassemia beta zero without crisis
- with
- with
- acute chest syndrome - D57.01 Hb-SS disease with acute chest syndrome
- cerebral vascular involvement - D57.03 Hb-SS disease with cerebral vascular involvement
- crisis (painful) - D57.00 Hb-SS disease with crisis, unspecified
- with complication specified NEC - D57.09 Hb-SS disease with crisis with other specified complication
- pain (vaso-occlusive) - D57.00 Hb-SS disease with crisis, unspecified
- splenic sequestration - D57.02 Hb-SS disease with splenic sequestration
- beta plus - D57.44 Sickle-cell thalassemia beta plus without crisis
- SC - D57.2 Sickle-cell/Hb-C disease
- SD - D57.8 Other sickle-cell disorders
- SE - D57.8 Other sickle-cell disorders
- spherocytosis - D58.0 Hereditary spherocytosis
- unstable, hemolytic - D58.2 Other hemoglobinopathies
- abnormal (mixed) NEC - D58.2 Other hemoglobinopathies
- hemolytic (newborn) - P55.9 Hemolytic disease of newborn, unspecified
- hemorrhagic - D69.9 Hemorrhagic condition, unspecified
- newborn - P53 Hemorrhagic disease of newborn
- Henoch (-Schönlein) (purpura nervosa) - D69.0 Allergic purpura
- hepatic - See: Disease, liver;
- hepatobiliary - K83.9 Disease of biliary tract, unspecified
- toxic - K71.9 Toxic liver disease, unspecified
- hepatolenticular - E83.01 Wilson's disease
- heredodegenerative NEC
- spinal cord - G95.89 Other specified diseases of spinal cord
- Hers' (glycogenosis VI) - E74.09 Other glycogen storage disease
- Herter (-Gee) (-Heubner) (nontropical sprue) - K90.0 Celiac disease
- Heubner-Herter (nontropical sprue) - K90.0 Celiac disease
- high fetal gene or hemoglobin thalassemia - D56.9 Thalassemia, unspecified
- Hildenbrand's - See: Typhus;
- hip (joint) - M25.9 Joint disorder, unspecified
- His (-Werner) (trench fever) - A79.0 Trench fever
- Hodgson's - See Also: Aneurysm, aorta, thorax; - I71.20 Thoracic aortic aneurysm, without rupture, unspecified
- ruptured - See Also: Aneurysm, aorta, thorax, ruptured; - I71.10 Thoracic aortic aneurysm, ruptured, unspecified
- Holla - See: Spherocytosis;
- hookworm - B76.9 Hookworm disease, unspecified
- specified NEC - B76.8 Other hookworm diseases
- host-versus-graft - D89.813 Graft-versus-host disease, unspecified
- human immunodeficiency virus (HIV) - B20 Human immunodeficiency virus [HIV] disease
- Huntington's - G10 Huntington's disease
- with dementia - See Also: Dementia, in, diseases specified elsewhere; - G10 Huntington's disease
- Hunt's (herpetic geniculate ganglionitis) (neuralgia) - B02.21 Postherpetic geniculate ganglionitis
- dyssynergia cerebellaris myoclonica - G11.19 Other early-onset cerebellar ataxia
- Hutchinson's (cheiropompholyx) - See: Hutchinson's disease;
- hyaline (diffuse) (generalized)
- hydatid - See: Echinococcus;
- hydroxyapatite deposition - M11.00 Hydroxyapatite deposition disease, unspecified site
- ankle - M11.07 Hydroxyapatite deposition disease, ankle and foot
- elbow - M11.02 Hydroxyapatite deposition disease, elbow
- foot joint - M11.07 Hydroxyapatite deposition disease, ankle and foot
- hand joint - M11.04 Hydroxyapatite deposition disease, hand
- hip - M11.05 Hydroxyapatite deposition disease, hip
- knee - M11.06 Hydroxyapatite deposition disease, knee
- multiple site - M11.09 Hydroxyapatite deposition disease, multiple sites
- shoulder - M11.01 Hydroxyapatite deposition disease, shoulder
- vertebra - M11.08 Hydroxyapatite deposition disease, vertebrae
- wrist - M11.03 Hydroxyapatite deposition disease, wrist
- hyperkinetic - See: Hyperkinesia;
- hypertensive - See: Hypertension;
- hypophysis - E23.7 Disorder of pituitary gland, unspecified
- Iceland - G93.39 Other post infection and related fatigue syndromes
- I-cell - E77.0 Defects in post-translational modification of lysosomal enzymes
- immune - D89.9 Disorder involving the immune mechanism, unspecified
- immunoproliferative (malignant) - C88.9 Malignant immunoproliferative disease, unspecified
- inclusion - B25.9 Cytomegaloviral disease, unspecified
- salivary gland - B25.9 Cytomegaloviral disease, unspecified
- infectious, infective - B99.9 Unspecified infectious disease
- inflammatory
- intervertebral disc - See Also: Disorder, disc;
- cervical, cervicothoracic - See: Disorder, disc, cervical;
- with
- myelopathy - See: Disorder, disc, cervical, with myelopathy;
- neuritis, radiculitis or radiculopathy - See: Disorder, disc, cervical, with neuritis;
- specified NEC - See: Disorder, disc, cervical, specified type NEC;
- with
- lumbar (with)
- lumbosacral (with)
- specified NEC - See: Disorder, disc, specified NEC;
- thoracic (with)
- thoracolumbar (with)
- with myelopathy - See: Disorder, disc, with, myelopathy;
- cervical, cervicothoracic - See: Disorder, disc, cervical;
- intestine - K63.9 Disease of intestine, unspecified
- iris - H21.9 Unspecified disorder of iris and ciliary body
- specified NEC - H21.89 Other specified disorders of iris and ciliary body
- iron metabolism or storage - E83.10 Disorder of iron metabolism, unspecified
- island (scrub typhus) - A75.3 Typhus fever due to Rickettsia tsutsugamushi
- itai-itai - See: Poisoning, cadmium;
- Jakob-Creutzfeldt - See: Creutzfeldt-Jakob disease or syndrome;
- jaw - M27.9 Disease of jaws, unspecified
- jigger - B88.1 Tungiasis [sandflea infestation]
- joint - See Also: Disorder, joint;
- Charcot's - See: Arthropathy, neuropathic (Charcot);
- degenerative - See: Osteoarthritis;
- multiple - M15.9 Polyosteoarthritis, unspecified
- spine - See: Spondylosis;
- facet joint - See Also: Spondylosis; - M47.819 Spondylosis without myelopathy or radiculopathy, site unspecified
- hypertrophic - See: Osteoarthritis;
- sacroiliac - M53.3 Sacrococcygeal disorders, not elsewhere classified
- specified NEC - See: Disorder, joint, specified type NEC;
- spine NEC - See: Dorsopathy;
- suppurative - See: Arthritis, pyogenic or pyemic;
- Jourdain's (acute gingivitis) - K05.00 Acute gingivitis, plaque induced
- Kaschin-Beck (endemic polyarthritis) - M12.10 Kaschin-Beck disease, unspecified site
- ankle - M12.17 Kaschin-Beck disease, ankle and foot
- elbow - M12.12 Kaschin-Beck disease, elbow
- foot joint - M12.17 Kaschin-Beck disease, ankle and foot
- hand joint - M12.14 Kaschin-Beck disease, hand
- hip - M12.15 Kaschin-Beck disease, hip
- knee - M12.16 Kaschin-Beck disease, knee
- multiple site - M12.19 Kaschin-Beck disease, multiple sites
- shoulder - M12.11 Kaschin-Beck disease, shoulder
- vertebra - M12.18 Kaschin-Beck disease, vertebrae
- wrist - M12.13 Kaschin-Beck disease, wrist
- Katayama - B65.2 Schistosomiasis due to Schistosoma japonicum
- Kedani (scrub typhus) - A75.3 Typhus fever due to Rickettsia tsutsugamushi
- Keshan - E59 Dietary selenium deficiency
- kidney (functional) (pelvis) - N28.9 Disorder of kidney and ureter, unspecified
- chronic - N18.9 Chronic kidney disease, unspecified
- hypertensive - See: Hypertension, kidney;
- stage 1 - N18.1 Chronic kidney disease, stage 1
- stage 2 (mild) - N18.2 Chronic kidney disease, stage 2 (mild)
- stage 3 (moderate) - N18.30 Chronic kidney disease, stage 3 unspecified
- stage 3a - N18.31 Chronic kidney disease, stage 3a
- stage 3b - N18.32 Chronic kidney disease, stage 3b
- stage 4 (severe) - N18.4 Chronic kidney disease, stage 4 (severe)
- stage 5 - N18.5 Chronic kidney disease, stage 5
- complicating pregnancy - See: Pregnancy, complicated by, renal disease;
- cystic (congenital) - Q61.9 Cystic kidney disease, unspecified
- diabetic - See: E08-E13 with .22;
- fibrocystic (congenital) - Q61.8 Other cystic kidney diseases
- hypertensive - See: Hypertension, kidney;
- in (due to)
- schistosomiasis (bilharziasis) - B65.9 Schistosomiasis, unspecified
- multicystic - Q61.4 Renal dysplasia
- polycystic - Q61.3 Polycystic kidney, unspecified
- chronic - N18.9 Chronic kidney disease, unspecified
- Kimmelstiel (-Wilson) (intercapillary polycystic (congenital) glomerulosclerosis) - See: E08-E13 with .21;
- Kimura - D21.9 Benign neoplasm of connective and other soft tissue, unspecified
- specified site (see Neoplasm, connective tissue benign)
- Kinnier Wilson's (hepatolenticular degeneration) - E83.01 Wilson's disease
- kissing - See: Mononucleosis, infectious;
- Klebs' - See Also: Glomerulonephritis; - N05.
- Klippel-Feil (brevicollis) - Q76.1 Klippel-Feil syndrome
- Köhler-Pellegrini-Stieda (calcification, knee joint) - See: Bursitis, tibial collateral;
- Kok - Q89.8 Other specified congenital malformations
- König's (osteochondritis dissecans) - See: Osteochondritis, dissecans;
- Korsakoff's (nonalcoholic) - F04 Amnestic disorder due to known physiological condition
- Kostmann's (infantile genetic agranulocytosis) - D70.0 Congenital agranulocytosis
- kuru - A81.81 Kuru
- Kyasanur Forest - A98.2 Kyasanur Forest disease
- labyrinth, ear - See: Disorder, ear, inner;
- lacrimal system - See: Disorder, lacrimal system;
- Lafora body - See Also: Epilepsy, progressive, Lafora; - G40.C09 Lafora progressive myoclonus epilepsy, not intractable, without status epilepticus
- Lancereaux-Mathieu (leptospiral jaundice) - A27.0 Leptospirosis icterohemorrhagica
- Landry's - G61.0 Guillain-Barre syndrome
- Larrey-Weil (leptospiral jaundice) - A27.0 Leptospirosis icterohemorrhagica
- larynx - J38.7 Other diseases of larynx
- legionnaires' - A48.1 Legionnaires' disease
- nonpneumonic - A48.2 Nonpneumonic Legionnaires' disease [Pontiac fever]
- Lenegre's - I44.2 Atrioventricular block, complete
- lens - H27.9 Unspecified disorder of lens
- specified NEC - H27.8 Other specified disorders of lens
- Lev's (acquired complete heart block) - I44.2 Atrioventricular block, complete
- Lewy body (dementia) - See Also: Dementia, in, diseases specified elsewhere; - G31.83 Neurocognitive disorder with Lewy bodies
- with behavioral disturbance - See Also: Dementia, in, diseases specified elsewhere; - G31.83 Neurocognitive disorder with Lewy bodies
- Lichtheim's (subacute combined sclerosis with pernicious anemia) - D51.0 Vitamin B12 deficiency anemia due to intrinsic factor deficiency
- Lightwood's (renal tubular acidosis) - N25.89 Other disorders resulting from impaired renal tubular function
- Lignac's (cystinosis) - E72.04 Cystinosis
- lip - K13.0 Diseases of lips
- lipid-storage - E75.6 Lipid storage disorder, unspecified
- specified NEC - E75.5 Other lipid storage disorders
- Lipschütz's - N76.6 Ulceration of vulva
- liver (chronic) (organic) - K76.9 Liver disease, unspecified
- alcoholic (chronic) - K70.9 Alcoholic liver disease, unspecified
- acute - See: Disease, liver, alcoholic, hepatitis;
- cirrhosis - K70.30 Alcoholic cirrhosis of liver without ascites
- with ascites - K70.31 Alcoholic cirrhosis of liver with ascites
- failure - K70.40 Alcoholic hepatic failure without coma
- with coma - K70.41 Alcoholic hepatic failure with coma
- fatty liver - K70.0 Alcoholic fatty liver
- fibrosis - K70.2 Alcoholic fibrosis and sclerosis of liver
- hepatitis - K70.10 Alcoholic hepatitis without ascites
- with ascites - K70.11 Alcoholic hepatitis with ascites
- sclerosis - K70.2 Alcoholic fibrosis and sclerosis of liver
- cystic, congenital - Q44.6 Cystic disease of liver
- drug-induced (idiosyncratic) (toxic) (predictable) (unpredictable) - See: Disease, liver, toxic;
- end stage - K72.1 Chronic hepatic failure
- due to hepatitis - See: Hepatitis;
- with coma - K72.11 Chronic hepatic failure with coma
- fatty, nonalcoholic (NAFLD) - K76.0 Fatty (change of) liver, not elsewhere classified
- alcoholic - K70.0 Alcoholic fatty liver
- fibrocystic (congenital) - Q44.6 Cystic disease of liver
- fluke
- gestational alloimmune (GALD) - P78.84 Gestational alloimmune liver disease
- glycogen storage - E74.09 Other glycogen storage disease
- in (due to)
- schistosomiasis (bilharziasis) - B65.9 Schistosomiasis, unspecified
- inflammatory - K75.9 Inflammatory liver disease, unspecified
- polycystic (congenital) - Q44.6 Cystic disease of liver
- toxic - K71.9 Toxic liver disease, unspecified
- with
- cholestasis - K71.0 Toxic liver disease with cholestasis
- cirrhosis (liver) - K71.7 Toxic liver disease with fibrosis and cirrhosis of liver
- fibrosis (liver) - K71.7 Toxic liver disease with fibrosis and cirrhosis of liver
- focal nodular hyperplasia - K71.8 Toxic liver disease with other disorders of liver
- hepatic granuloma - K71.8 Toxic liver disease with other disorders of liver
- hepatic necrosis - K71.10 Toxic liver disease with hepatic necrosis, without coma
- with coma - K71.11 Toxic liver disease with hepatic necrosis, with coma
- hepatitis NEC - K71.6 Toxic liver disease with hepatitis, not elsewhere classified
- acute - K71.2 Toxic liver disease with acute hepatitis
- chronic
- active - K71.50 Toxic liver disease with chronic active hepatitis without ascites
- with ascites - K71.51 Toxic liver disease with chronic active hepatitis with ascites
- lobular - K71.4 Toxic liver disease with chronic lobular hepatitis
- persistent - K71.3 Toxic liver disease with chronic persistent hepatitis
- active - K71.50 Toxic liver disease with chronic active hepatitis without ascites
- lupoid - K71.50 Toxic liver disease with chronic active hepatitis without ascites
- with ascites - K71.51 Toxic liver disease with chronic active hepatitis with ascites
- peliosis hepatis - K71.8 Toxic liver disease with other disorders of liver
- veno-occlusive disease (VOD) of liver - K71.8 Toxic liver disease with other disorders of liver
- with
- veno-occlusive - K76.5 Hepatic veno-occlusive disease
- alcoholic (chronic) - K70.9 Alcoholic liver disease, unspecified
- Lobo's (keloid blastomycosis) - B48.0 Lobomycosis
- Lobstein's (brittle bones and blue sclera) - Q78.0 Osteogenesis imperfecta
- Ludwig's (submaxillary cellulitis) - K12.2 Cellulitis and abscess of mouth
- lumbosacral region - M53.87 Other specified dorsopathies, lumbosacral region
- lung - J98.4 Other disorders of lung
- black - J60 Coalworker's pneumoconiosis
- congenital - Q33.9 Congenital malformation of lung, unspecified
- cystic - J98.4 Other disorders of lung
- congenital - Q33.0 Congenital cystic lung
- fibroid (chronic) - See: Fibrosis, lung;
- fluke - B66.4 Paragonimiasis
- oriental - B66.4 Paragonimiasis
- in
- interstitial - J84.9 Interstitial pulmonary disease, unspecified
- drug-induced - See: Disorder, lung, interstitial, drug-induced;
- of childhood, specified NEC - J84.848 Other interstitial lung diseases of childhood
- drug-induced - See: Disorder, lung, interstitial, drug-induced;
- respiratory bronchiolitis - J84.115 Respiratory bronchiolitis interstitial lung disease
- specified NEC - J84.89 Other specified interstitial pulmonary diseases
- with progressive fibrotic phenotype, in diseases classified elsewhere - J84.170 Interstitial lung disease with progressive fibrotic phenotype in diseases classified elsewhere
- obstructive (chronic) - J44.9 Chronic obstructive pulmonary disease, unspecified
- decompensated - J44.1 Chronic obstructive pulmonary disease with (acute) exacerbation
- with
- exacerbation (acute) - J44.1 Chronic obstructive pulmonary disease with (acute) exacerbation
- with
- with
- acute
- alveolitis, allergic - J67.9 Hypersensitivity pneumonitis due to unspecified organic dust
- asthma - J44.89 Other specified chronic obstructive pulmonary disease
- bronchiectasis - J47.9 Bronchiectasis, uncomplicated
- bronchitis - J44.89 Other specified chronic obstructive pulmonary disease
- emphysema - J43.9 Emphysema, unspecified
- hypersensitivity pneumonitis - J67.9 Hypersensitivity pneumonitis due to unspecified organic dust
- decompensated - J44.1 Chronic obstructive pulmonary disease with (acute) exacerbation
- polycystic - J98.4 Other disorders of lung
- congenital - Q33.0 Congenital cystic lung
- rheumatoid (diffuse) (interstitial) - See: Rheumatoid, lung;
- vaping (associated) (device) (product) (use) - U07.0 Vaping-related disorder
- Lutembacher's (atrial septal defect with mitral stenosis) - Q21.19 Other specified atrial septal defect
- Lyme - A69.20 Lyme disease, unspecified
- lymphatic (gland) (system) (channel) (vessel) - I89.9 Noninfective disorder of lymphatic vessels and lymph nodes, unspecified
- lymphoproliferative - D47.9 Neoplasm of uncertain behavior of lymphoid, hematopoietic and related tissue, unspecified
- specified NEC - D47.Z9 Other specified neoplasms of uncertain behavior of lymphoid, hematopoietic and related tissue
- T-gamma - D47.Z9 Other specified neoplasms of uncertain behavior of lymphoid, hematopoietic and related tissue
- X-linked - D82.3 Immunodeficiency following hereditary defective response to Epstein-Barr virus
- Magitot's - M27.2 Inflammatory conditions of jaws
- malarial - See: Malaria;
- malignant - See Also: Neoplasm, malignant, by site;
- Manson's - B65.1 Schistosomiasis due to Schistosoma mansoni [intestinal schistosomiasis]
- maple bark - J67.6 Maple-bark-stripper's lung
- maple-syrup-urine - E71.0 Maple-syrup-urine disease
- Marburg (virus) - A98.3 Marburg virus disease
- Marion's (bladder neck obstruction) - N32.0 Bladder-neck obstruction
- Marsh's (exophthalmic goiter) - See: Hyperthyroidism, with, goiter (diffuse);
- mastoid (process) - See: Disorder, ear, middle;
- Mathieu's (leptospiral jaundice) - A27.0 Leptospirosis icterohemorrhagica
- Maxcy's - A75.2 Typhus fever due to Rickettsia typhi
- McArdle (-Schmid-Pearson) (glycogenosis V) - E74.04 McArdle disease
- mediastinum - J98.59 Other diseases of mediastinum, not elsewhere classified
- medullary center (idiopathic) (respiratory) - G93.89 Other specified disorders of brain
- Meige's (chronic hereditary edema) - Q82.0 Hereditary lymphedema
- meningococcal - See: Infection, meningococcal;
- mental - F99 Mental disorder, not otherwise specified
- organic - F09 Unspecified mental disorder due to known physiological condition
- mesenchymal - M35.9 Systemic involvement of connective tissue, unspecified
- mesenteric embolic - See Also: Ischemia, intestine, acute; - K55.039 Acute (reversible) ischemia of large intestine, extent unspecified
- metabolic, metabolism - E88.9 Metabolic disorder, unspecified
- bilirubin - E80.7 Disorder of bilirubin metabolism, unspecified
- metal-polisher's - J62.8 Pneumoconiosis due to other dust containing silica
- metastatic - See Also: Neoplasm, secondary, by site; - C79.9 Secondary malignant neoplasm of unspecified site
- microvascular - code to condition
- microvillus
- middle ear - See: Disorder, ear, middle;
- Mikulicz' (dryness of mouth, absent or decreased lacrimation) - K11.8 Other diseases of salivary glands
- Milroy's (chronic hereditary edema) - Q82.0 Hereditary lymphedema
- Minamata - See: Poisoning, mercury;
- minicore - G71.29 Other congenital myopathy
- Minor's - G95.19 Other vascular myelopathies
- Minot's (hemorrhagic disease, newborn) - P53 Hemorrhagic disease of newborn
- Minot-von Willebrand-Jürgens (angiohemophilia) - See: Disease, von Willebrand;
- Mitchell's (erythromelalgia) - I73.81 Erythromelalgia
- mitral (valve) - I05.9 Rheumatic mitral valve disease, unspecified
- nonrheumatic - I34.9 Nonrheumatic mitral valve disorder, unspecified
- mixed connective tissue - M35.1 Other overlap syndromes
- MOG antibody - G37.81 Myelin oligodendrocyte glycoprotein antibody disease
- moldy hay - J67.0 Farmer's lung
- Monge's - T70.29 Other effects of high altitude
- Morgagni-Adams-Stokes (syncope with heart block) - I45.9 Conduction disorder, unspecified
- Morgagni's (syndrome) (hyperostosis frontalis interna) - M85.2 Hyperostosis of skull
- Morton's (with metatarsalgia) - See: Lesion, nerve, plantar;
- Morvan's - G60.8 Other hereditary and idiopathic neuropathies
- motor neuron (bulbar) (mixed type) (spinal) - G12.20 Motor neuron disease, unspecified
- moyamoya - I67.5 Moyamoya disease
- mu heavy chain disease - C88.2 Heavy chain disease
- multicore - G71.29 Other congenital myopathy
- multiminicore - G71.29 Other congenital myopathy
- muscle - See Also: Disorder, muscle;
- inflammatory - See: Myositis;
- ocular (external) - See: Strabismus;
- musculoskeletal system, soft tissue - See: also Disorder, soft tissue;
- specified NEC - See: Disorder, soft tissue, specified type NEC;
- mushroom workers' - J67.5 Mushroom-worker's lung
- mycotic - B49 Unspecified mycosis
- myelin oligodendrocyte glycoprotein antibody - G37.81 Myelin oligodendrocyte glycoprotein antibody disease
- myelodysplastic - See Also: Syndrome, myelodysplastic; - C94.6 Myelodysplastic disease, not elsewhere classified
- myelodysplastic/myeloproliferative neoplasm, unclassifiable - C94.6 Myelodysplastic disease, not elsewhere classified
- myeloproliferative - D47.1 Chronic myeloproliferative disease
- myocardium, myocardial - See Also: Degeneration, myocardial; - I51.5 Myocardial degeneration
- primary (idiopathic) - I42.9 Cardiomyopathy, unspecified
- myoneural - G70.9 Myoneural disorder, unspecified
- Naegeli's - D69.1 Qualitative platelet defects
- nails - L60.9 Nail disorder, unspecified
- specified NEC - L60.8 Other nail disorders
- Nairobi (sheep virus) - A93.8 Other specified arthropod-borne viral fevers
- nasal - J34.9 Unspecified disorder of nose and nasal sinuses
- nemaline body - G71.21 Nemaline myopathy
- nerve - See: Disorder, nerve;
- nervous system - G98.8 Other disorders of nervous system
- autonomic - G90.9 Disorder of the autonomic nervous system, unspecified
- central - G96.9 Disorder of central nervous system, unspecified
- specified NEC - G96.89 Other specified disorders of central nervous system
- congenital - Q07.9 Congenital malformation of nervous system, unspecified
- parasympathetic - G90.9 Disorder of the autonomic nervous system, unspecified
- specified NEC - G98.8 Other disorders of nervous system
- sympathetic - G90.9 Disorder of the autonomic nervous system, unspecified
- vegetative - G90.9 Disorder of the autonomic nervous system, unspecified
- neuromuscular system - G70.9 Myoneural disorder, unspecified
- Newcastle - B30.8 Other viral conjunctivitis
- Nicolas (-Durand)-Favre (climatic bubo) - A55 Chlamydial lymphogranuloma (venereum)
- nipple - N64.9 Disorder of breast, unspecified
- Nishimoto (-Takeuchi) - I67.5 Moyamoya disease
- nonautoimmune hemolytic - D59.4 Other nonautoimmune hemolytic anemias
- drug-induced - D59.2 Drug-induced nonautoimmune hemolytic anemia
- Nonne-Milroy-Meige (chronic hereditary edema) - Q82.0 Hereditary lymphedema
- nose - J34.9 Unspecified disorder of nose and nasal sinuses
- nucleus pulposus - See: Disorder, disc;
- nutritional - E63.9 Nutritional deficiency, unspecified
- oast-house-urine - E72.19 Other disorders of sulfur-bearing amino-acid metabolism
- ocular
- zoster - B02.30 Zoster ocular disease, unspecified
- ocular
- obliterative vascular - I77.1 Stricture of artery
- Ohara's - See: Tularemia;
- Opitz's (congestive splenomegaly) - D73.2 Chronic congestive splenomegaly
- Oppenheim-Urbach (necrobiosis lipoidica diabeticorum) - See: E08-E13 with .620;
- optic nerve NEC - See: Disorder, nerve, optic;
- orbit - See: Disorder, orbit;
- organ
- vaping (associated) (device) (product) (use) - U07.0 Vaping-related disorder
- Oriental liver fluke - B66.1 Clonorchiasis
- Oriental lung fluke - B66.4 Paragonimiasis
- Ormond's - N13.5 Crossing vessel and stricture of ureter without hydronephrosis
- Oropouche virus - A93.0 Oropouche virus disease
- Osler-Rendu (familial hemorrhagic telangiectasia) - I78.0 Hereditary hemorrhagic telangiectasia
- osteofibrocystic - E21.0 Primary hyperparathyroidism
- Otto's - M24.7 Protrusio acetabuli
- outer ear - See: Disorder, ear, external;
- ovary (noninflammatory) - N83.9 Noninflammatory disorder of ovary, fallopian tube and broad ligament, unspecified
- Owren's (congenital) - See: Defect, coagulation;
- p110d-activating mutation causing senescent T cells, lymphadenopathy, and immunodeficiency [PASLI] - D81.82 Activated Phosphoinositide 3-kinase Delta Syndrome [APDS]
- pancreas - K86.9 Disease of pancreas, unspecified
- panvalvular - I08.9 Rheumatic multiple valve disease, unspecified
- specified NEC - I08.8 Other rheumatic multiple valve diseases
- parametrium (noninflammatory) - N83.9 Noninflammatory disorder of ovary, fallopian tube and broad ligament, unspecified
- parasitic - B89 Unspecified parasitic disease
- parathyroid (gland) - E21.5 Disorder of parathyroid gland, unspecified
- specified NEC - E21.4 Other specified disorders of parathyroid gland
- Parkinson's - G20.A1 Parkinson's disease without dyskinesia, without mention of fluctuations
- with dyskinesia
- with
- without mention of
- without dyskinesia
- with
- without mention of
- with dyskinesia
- parodontal - K05.6 Periodontal disease, unspecified
- Parrot's (syphilitic osteochondritis) - A50.02 Early congenital syphilitic osteochondropathy
- Parry's (exophthalmic goiter) - See: Hyperthyroidism, with, goiter (diffuse);
- Parson's (exophthalmic goiter) - See: Hyperthyroidism, with, goiter (diffuse);
- Paxton's (white piedra) - B36.2 White piedra
- pearl-worker's - See: Osteomyelitis, specified type NEC;
- Pellegrini-Stieda (calcification, knee joint) - See: Bursitis, tibial collateral;
- pelvis, pelvic
- female NOS - N94.9 Unspecified condition associated with female genital organs and menstrual cycle
- specified NEC - N94.89 Other specified conditions associated with female genital organs and menstrual cycle
- gonococcal (acute) (chronic) - A54.24 Gonococcal female pelvic inflammatory disease
- inflammatory (female) - N73.9 Female pelvic inflammatory disease, unspecified
- acute - N73.0 Acute parametritis and pelvic cellulitis
- chlamydial - A56.11 Chlamydial female pelvic inflammatory disease
- chronic - N73.1 Chronic parametritis and pelvic cellulitis
- specified NEC - N73.8 Other specified female pelvic inflammatory diseases
- syphilitic (secondary) - A51.42 Secondary syphilitic female pelvic disease
- late - A52.76 Other genitourinary symptomatic late syphilis
- tuberculous - A18.17 Tuberculous female pelvic inflammatory disease
- organ, female - N94.9 Unspecified condition associated with female genital organs and menstrual cycle
- peritoneum, female NEC - N94.89 Other specified conditions associated with female genital organs and menstrual cycle
- female NOS - N94.9 Unspecified condition associated with female genital organs and menstrual cycle
- penis - N48.9 Disorder of penis, unspecified
- periapical tissues NOS - K04.90 Unspecified diseases of pulp and periapical tissues
- periodontal - K05.6 Periodontal disease, unspecified
- specified NEC - K05.5 Other periodontal diseases
- periosteum - See: Disorder, bone, specified type NEC;
- peripheral
- arterial - I73.9 Peripheral vascular disease, unspecified
- autonomic nervous system - G90.9 Disorder of the autonomic nervous system, unspecified
- nerves - See: Polyneuropathy;
- vascular NOS - I73.9 Peripheral vascular disease, unspecified
- in diabetes mellitus - See: Diabetes, by type, with peripheral angiopathy;
- peritoneum - K66.9 Disorder of peritoneum, unspecified
- persistent mucosal (middle ear) - H66.20 Chronic atticoantral suppurative otitis media, unspecified ear
- Petit's - See: Hernia, abdomen, specified site NEC;
- pharynx - J39.2 Other diseases of pharynx
- specified NEC - J39.2 Other diseases of pharynx
- Phocas' - See: Mastopathy, cystic;
- photochromogenic (acid-fast bacilli) (pulmonary) - A31.0 Pulmonary mycobacterial infection
- nonpulmonary - A31.9 Mycobacterial infection, unspecified
- Pick's - See Also: Dementia, in, diseases specified elsewhere; - G31.01 Pick's disease
- brain - See Also: Dementia, in, diseases specified elsewhere; - G31.01 Pick's disease
- with behavioral disturbance - See Also: Dementia, in, diseases specified elsewhere; - G31.01 Pick's disease
- of pericardium (pericardial pseudocirrhosis of liver) - I31.1 Chronic constrictive pericarditis
- with behavioral disturbance - See Also: Dementia, in, diseases specified elsewhere; - G31.01 Pick's disease
- brain - See Also: Dementia, in, diseases specified elsewhere; - G31.01 Pick's disease
- pigeon fancier's - J67.2 Bird fancier's lung
- pineal gland - E34.8 Other specified endocrine disorders
- pink - See: Poisoning, mercury;
- Pinkus' (lichen nitidus) - L44.1 Lichen nitidus
- pinworm - B80 Enterobiasis
- Piry virus - A93.8 Other specified arthropod-borne viral fevers
- pituitary (gland) - E23.7 Disorder of pituitary gland, unspecified
- pituitary-snuff-taker's - J67.8 Hypersensitivity pneumonitis due to other organic dusts
- pleura (cavity) - J94.9 Pleural condition, unspecified
- specified NEC - J94.8 Other specified pleural conditions
- pneumatic drill (hammer) - T75.21 Pneumatic hammer syndrome
- Pollitzer's (hidradenitis suppurativa) - L73.2 Hidradenitis suppurativa
- polycystic
- polyethylene - T84.05 Periprosthetic osteolysis of internal prosthetic joint
- Pompe's (glycogenosis II) - E74.02 Pompe disease
- Posadas-Wernicke - B38.9 Coccidioidomycosis, unspecified
- Potain's (pulmonary edema) - See: Edema, lung;
- prepuce - N47.8 Other disorders of prepuce
- Pringle's (tuberous sclerosis) - Q85.1 Tuberous sclerosis
- prion, central nervous system - A81.9 Atypical virus infection of central nervous system, unspecified
- specified NEC - A81.89 Other atypical virus infections of central nervous system
- prostate - N42.9 Disorder of prostate, unspecified
- specified NEC - N42.89 Other specified disorders of prostate
- protozoal - B64 Unspecified protozoal disease
- acanthamebiasis - See: Acanthamebiasis;
- African trypanosomiasis - See: African trypanosomiasis;
- babesiosis - See Also: Babesiosis; - B60.00 Babesiosis, unspecified
- Chagas disease - See: Chagas disease;
- intestine, intestinal - A07.9 Protozoal intestinal disease, unspecified
- leishmaniasis - See: Leishmaniasis;
- malaria - See: Malaria;
- naegleriasis - B60.2 Naegleriasis
- pneumocystosis - B59 Pneumocystosis
- specified organism NEC - B60.8 Other specified protozoal diseases
- toxoplasmosis - See: Toxoplasmosis;
- pseudo-Hurler's - E77.0 Defects in post-translational modification of lysosomal enzymes
- psychiatric - F99 Mental disorder, not otherwise specified
- psychotic - See: Psychosis;
- Puente's (simple glandular cheilitis) - K13.0 Diseases of lips
- puerperal - See Also: Puerperal; - O90.89 Other complications of the puerperium, not elsewhere classified
- pulmonary - See Also: Disease, lung;
- artery - I28.9 Disease of pulmonary vessels, unspecified
- chronic obstructive - J44.9 Chronic obstructive pulmonary disease, unspecified
- decompensated - J44.1 Chronic obstructive pulmonary disease with (acute) exacerbation
- with
- exacerbation (acute) - J44.1 Chronic obstructive pulmonary disease with (acute) exacerbation
- with
- with
- acute bronchitis - J44.0 Chronic obstructive pulmonary disease with (acute) lower respiratory infection
- exacerbation (acute) - J44.1 Chronic obstructive pulmonary disease with (acute) exacerbation
- lower respiratory infection (acute) - J44.0 Chronic obstructive pulmonary disease with (acute) lower respiratory infection
- decompensated - J44.1 Chronic obstructive pulmonary disease with (acute) exacerbation
- heart - I27.9 Pulmonary heart disease, unspecified
- specified NEC - I27.89 Other specified pulmonary heart diseases
- hypertensive (vascular) - See Also: Hypertension, pulmonary; - I27.20 Pulmonary hypertension, unspecified
- primary (idiopathic) - I27.0 Primary pulmonary hypertension
- valve - I37.9 Nonrheumatic pulmonary valve disorder, unspecified
- rheumatic - I09.89 Other specified rheumatic heart diseases
- pulp (dental) NOS - K04.90 Unspecified diseases of pulp and periapical tissues
- pulseless - M31.4 Aortic arch syndrome [Takayasu]
- Putnam's (subacute combined sclerosis with pernicious anemia) - D51.0 Vitamin B12 deficiency anemia due to intrinsic factor deficiency
- Pyle (-Cohn) (metaphyseal dysplasia) - Q78.5 Metaphyseal dysplasia
- ragpicker's or ragsorter's - A22.1 Pulmonary anthrax
- Raynaud's - See: Raynaud's disease;
- reactive airway - See: Asthma;
- Reclus' (cystic) - See: Mastopathy, cystic;
- rectum - K62.9 Disease of anus and rectum, unspecified
- specified NEC - K62.89 Other specified diseases of anus and rectum
- Refsum's (heredopathia atactica polyneuritiformis) - G60.1 Refsum's disease
- renal (functional) (pelvis) - See Also: Disease, kidney; - N28.9 Disorder of kidney and ureter, unspecified
- acute - N28.9 Disorder of kidney and ureter, unspecified
- chronic - See Also: Disease, kidney, chronic; - N18.9 Chronic kidney disease, unspecified
- cystic, congenital - Q61.9 Cystic kidney disease, unspecified
- diabetic - See: E08-E13 with .22;
- end-stage (failure) - N18.6 End stage renal disease
- due to hypertension - I12.0 Hypertensive chronic kidney disease with stage 5 chronic kidney disease or end stage renal disease
- fibrocystic (congenital) - Q61.8 Other cystic kidney diseases
- hypertensive - See: Hypertension, kidney;
- lupus - M32.14 Glomerular disease in systemic lupus erythematosus
- phosphate-losing (tubular) - N25.0 Renal osteodystrophy
- polycystic (congenital) - Q61.3 Polycystic kidney, unspecified
- rapidly progressive - N01.9 Rapidly progressive nephritic syndrome with unspecified morphologic changes
- subacute - N01.9 Rapidly progressive nephritic syndrome with unspecified morphologic changes
- with
- edema - See: Nephrosis;
- glomerular lesion - See: Glomerulonephritis;
- with edema - See: Nephrosis;
- interstitial nephritis - N12 Tubulo-interstitial nephritis, not specified as acute or chronic
- Rendu-Osler-Weber (familial hemorrhagic telangiectasia) - I78.0 Hereditary hemorrhagic telangiectasia
- renovascular (arteriosclerotic) - See: Hypertension, kidney;
- respiratory (tract) - J98.9 Respiratory disorder, unspecified
- acute or subacute NOS - J06.9 Acute upper respiratory infection, unspecified
- due to
- chemicals, gases, fumes or vapors (inhalation) - J68.3 Other acute and subacute respiratory conditions due to chemicals, gases, fumes and vapors
- external agent - J70.9 Respiratory conditions due to unspecified external agent
- specified NEC - J70.8 Respiratory conditions due to other specified external agents
- radiation - J70.0 Acute pulmonary manifestations due to radiation
- smoke inhalation - J70.5 Respiratory conditions due to smoke inhalation
- noninfectious - J39.8 Other specified diseases of upper respiratory tract
- due to
- chronic NOS - J98.9 Respiratory disorder, unspecified
- due to
- chemicals, gases, fumes or vapors - J68.4 Chronic respiratory conditions due to chemicals, gases, fumes and vapors
- external agent - J70.9 Respiratory conditions due to unspecified external agent
- specified NEC - J70.8 Respiratory conditions due to other specified external agents
- radiation - J70.1 Chronic and other pulmonary manifestations due to radiation
- newborn - P27.9 Unspecified chronic respiratory disease originating in the perinatal period
- specified NEC - P27.8 Other chronic respiratory diseases originating in the perinatal period
- due to
- due to
- newborn - P28.9 Respiratory condition of newborn, unspecified
- specified type NEC - P28.89 Other specified respiratory conditions of newborn
- upper - J39.9 Disease of upper respiratory tract, unspecified
- acute or subacute NOS - J06.9 Acute upper respiratory infection, unspecified
- retina, retinal - H35.9 Unspecified retinal disorder
- rheumatoid - See: Arthritis, rheumatoid;
- rickettsial NOS - A79.9 Rickettsiosis, unspecified
- specified type NEC - A79.89 Other specified rickettsioses
- Riga (-Fede) (cachectic aphthae) - K14.0 Glossitis
- Riggs' (compound periodontitis) - See: Periodontitis;
- Ritter's - L00 Staphylococcal scalded skin syndrome
- Rivalta's (cervicofacial actinomycosis) - A42.2 Cervicofacial actinomycosis
- Robles' (onchocerciasis) - B73.01 Onchocerciasis with endophthalmitis
- rod body - G71.21 Nemaline myopathy
- Roger's (congenital interventricular septal defect) - Q21.0 Ventricular septal defect
- Rosenthal's (factor XI deficiency) - D68.1 Hereditary factor XI deficiency
- Ross River - B33.1 Ross River disease
- Rossbach's (hyperchlorhydria) - K31.89 Other diseases of stomach and duodenum
- psychogenic - F45.8 Other somatoform disorders
- Rotes Quérol - See: Hyperostosis, ankylosing;
- Roth (-Bernhardt) - See: Mononeuropathy, lower limb, meralgia paresthetica;
- Runeberg's (progressive pernicious anemia) - D51.0 Vitamin B12 deficiency anemia due to intrinsic factor deficiency
- sacroiliac NEC - M53.3 Sacrococcygeal disorders, not elsewhere classified
- salivary gland or duct - K11.9 Disease of salivary gland, unspecified
- sandworm - B76.9 Hookworm disease, unspecified
- Schimmelbusch's - See: Mastopathy, cystic;
- Schmorl's - See: Schmorl's disease or nodes;
- Schönlein (-Henoch) (purpura rheumatica) - D69.0 Allergic purpura
- Schottmüller's - See: Fever, paratyphoid;
- Schultz's (agranulocytosis) - See: Agranulocytosis;
- Schwalbe-Ziehen-Oppenheim - G24.1 Genetic torsion dystonia
- Schwartz-Jampel - G71.13 Myotonic chondrodystrophy
- sclera - H15.9 Unspecified disorder of sclera
- specified NEC - H15.89 Other disorders of sclera
- scrofulous (tuberculous) - A18.2 Tuberculous peripheral lymphadenopathy
- scrotum - N50.9 Disorder of male genital organs, unspecified
- sebaceous glands - L73.9 Follicular disorder, unspecified
- semilunar cartilage, cystic - See Also: Derangement, knee, meniscus, cystic;
- seminal vesicle - N50.9 Disorder of male genital organs, unspecified
- serum NEC - See Also: Reaction, serum; - T80.69 Other serum reaction due to other serum
- sexually transmitted - A64 Unspecified sexually transmitted disease
- anogenital
- warts - A63.0 Anogenital (venereal) warts
- chancroid - A57 Chancroid
- chlamydial infection - See: Chlamydia;
- gonorrhea - See: Gonorrhea;
- granuloma inguinale - A58 Granuloma inguinale
- specified organism NEC - A63.8 Other specified predominantly sexually transmitted diseases
- syphilis - See: Syphilis;
- trichomoniasis - See: Trichomoniasis;
- anogenital
- Sézary - C84.1 Sezary disease
- shimamushi (scrub typhus) - A75.3 Typhus fever due to Rickettsia tsutsugamushi
- shipyard - B30.0 Keratoconjunctivitis due to adenovirus
- sickle-cell - D57.1 Sickle-cell disease without crisis
- elliptocytosis - D57.8 Other sickle-cell disorders
- Hb-C - D57.20 Sickle-cell/Hb-C disease without crisis
- with
- acute chest syndrome - D57.211 Sickle-cell/Hb-C disease with acute chest syndrome
- cerebral vascular involvement - D57.213 Sickle-cell/Hb-C disease with cerebral vascular involvement
- crisis - D57.219 Sickle-cell/Hb-C disease with crisis, unspecified
- dactylitis - D57.214 Sickle-cell/Hb-C disease with dactylitis
- pain (vaso-occlusive) - D57.219 Sickle-cell/Hb-C disease with crisis, unspecified
- priapism - D57.218 Sickle-cell/Hb-C disease with crisis with other specified complication
- splenic sequestration - D57.212 Sickle-cell/Hb-C disease with splenic sequestration
- without crisis - D57.20 Sickle-cell/Hb-C disease without crisis
- with
- Hb-SD - D57.80 Other sickle-cell disorders without crisis
- with
- acute chest syndrome - D57.811 Other sickle-cell disorders with acute chest syndrome
- cerebral vascular involvement - D57.813 Other sickle-cell disorders with cerebral vascular involvement
- crisis - D57.819 Other sickle-cell disorders with crisis, unspecified
- dactylitis - D57.814 Other sickle-cell disorders with dactylitis
- pain (vaso-occlusive) - D57.819 Other sickle-cell disorders with crisis, unspecified
- splenic sequestration - D57.812 Other sickle-cell disorders with splenic sequestration
- without crisis - D57.80 Other sickle-cell disorders without crisis
- with
- Hb-SE - D57.80 Other sickle-cell disorders without crisis
- with
- acute chest syndrome - D57.811 Other sickle-cell disorders with acute chest syndrome
- cerebral vascular involvement - D57.813 Other sickle-cell disorders with cerebral vascular involvement
- crisis - D57.819 Other sickle-cell disorders with crisis, unspecified
- dactylitis - D57.814 Other sickle-cell disorders with dactylitis
- pain (vaso-occlusive) - D57.819 Other sickle-cell disorders with crisis, unspecified
- splenic sequestration - D57.812 Other sickle-cell disorders with splenic sequestration
- without crisis - D57.80 Other sickle-cell disorders without crisis
- with
- specified NEC - D57.80 Other sickle-cell disorders without crisis
- with
- acute chest syndrome - D57.811 Other sickle-cell disorders with acute chest syndrome
- cerebral vascular involvement - D57.813 Other sickle-cell disorders with cerebral vascular involvement
- crisis - D57.819 Other sickle-cell disorders with crisis, unspecified
- dactylitis - D57.814 Other sickle-cell disorders with dactylitis
- pain (vaso-occlusive) - D57.819 Other sickle-cell disorders with crisis, unspecified
- splenic sequestration - D57.812 Other sickle-cell disorders with splenic sequestration
- without crisis - D57.80 Other sickle-cell disorders without crisis
- with
- spherocytosis - D57.80 Other sickle-cell disorders without crisis
- with
- acute chest syndrome - D57.811 Other sickle-cell disorders with acute chest syndrome
- cerebral vascular involvement - D57.813 Other sickle-cell disorders with cerebral vascular involvement
- crisis - D57.819 Other sickle-cell disorders with crisis, unspecified
- with complication specified NEC - D57.818 Other sickle-cell disorders with crisis with other specified complication
- pain (vaso-occlusive) - D57.819 Other sickle-cell disorders with crisis, unspecified
- splenic sequestration - D57.812 Other sickle-cell disorders with splenic sequestration
- without crisis - D57.80 Other sickle-cell disorders without crisis
- with
- thalassemia - D57.40 Sickle-cell thalassemia without crisis
- beta plus - D57.44 Sickle-cell thalassemia beta plus without crisis
- with
- acute chest syndrome - D57.451 Sickle-cell thalassemia beta plus with acute chest syndrome
- with dactylitis - D57.454 Sickle-cell thalassemia beta plus with dactylitis
- cerebral vascular involvement - D57.453 Sickle-cell thalassemia beta plus with cerebral vascular involvement
- crisis - D57.459 Sickle-cell thalassemia beta plus with crisis, unspecified
- with specified complication NEC - D57.458 Sickle-cell thalassemia beta plus with crisis with other specified complication
- dactylitis - D57.454 Sickle-cell thalassemia beta plus with dactylitis
- pain (vaso-occlusive) - D57.459 Sickle-cell thalassemia beta plus with crisis, unspecified
- splenic sequestration - D57.452 Sickle-cell thalassemia beta plus with splenic sequestration
- acute chest syndrome - D57.451 Sickle-cell thalassemia beta plus with acute chest syndrome
- without crisis - D57.44 Sickle-cell thalassemia beta plus without crisis
- with
- beta zero - D57.42 Sickle-cell thalassemia beta zero without crisis
- with
- acute chest syndrome - D57.431 Sickle-cell thalassemia beta zero with acute chest syndrome
- with dactylitis - D57.434 Sickle-cell thalassemia beta zero with dactylitis
- cerebral vascular involvement - D57.433 Sickle-cell thalassemia beta zero with cerebral vascular involvement
- crisis - D57.439 Sickle-cell thalassemia beta zero with crisis, unspecified
- with specified complication NEC - D57.438 Sickle-cell thalassemia beta zero with crisis with other specified complication
- dactylitis - D57.434 Sickle-cell thalassemia beta zero with dactylitis
- pain (vaso-occlusive) - D57.439 Sickle-cell thalassemia beta zero with crisis, unspecified
- splenic sequestration - D57.432 Sickle-cell thalassemia beta zero with splenic sequestration
- acute chest syndrome - D57.431 Sickle-cell thalassemia beta zero with acute chest syndrome
- without crisis - D57.42 Sickle-cell thalassemia beta zero without crisis
- with
- with
- acute chest syndrome - D57.411 Sickle-cell thalassemia, unspecified, with acute chest syndrome
- cerebral vascular involvement - D57.413 Sickle-cell thalassemia, unspecified, with cerebral vascular involvement
- crisis (painful) - D57.419 Sickle-cell thalassemia, unspecified, with crisis
- with specified complication NEC - D57.418 Sickle-cell thalassemia, unspecified, with crisis with other specified complication
- dactylitis - D57.414 Sickle-cell thalassemia, unspecified, with dactylitis
- pain (vaso-occlusive) - D57.419 Sickle-cell thalassemia, unspecified, with crisis
- splenic sequestration - D57.412 Sickle-cell thalassemia, unspecified, with splenic sequestration
- without crisis - D57.40 Sickle-cell thalassemia without crisis
- beta plus - D57.44 Sickle-cell thalassemia beta plus without crisis
- with
- acute chest syndrome - D57.01 Hb-SS disease with acute chest syndrome
- cerebral vascular involvement - D57.03 Hb-SS disease with cerebral vascular involvement
- crisis (painful) - D57.00 Hb-SS disease with crisis, unspecified
- dactylitis - D57.04 Hb-SS disease with dactylitis
- pain (vaso-occlusive) - D57.00 Hb-SS disease with crisis, unspecified
- priapism - D57.09 Hb-SS disease with crisis with other specified complication
- splenic sequestration - D57.02 Hb-SS disease with splenic sequestration
- silo-filler's - J68.8 Other respiratory conditions due to chemicals, gases, fumes and vapors
- simian B - B00.4 Herpesviral encephalitis
- Simons' (progressive lipodystrophy) - E88.1 Lipodystrophy, not elsewhere classified
- sin nombre virus - B33.4 Hantavirus (cardio)-pulmonary syndrome [HPS] [HCPS]
- sinus - See: Sinusitis;
- Sirkari's - B55.0 Visceral leishmaniasis
- sixth - B08.20 Exanthema subitum [sixth disease], unspecified
- skin - L98.9 Disorder of the skin and subcutaneous tissue, unspecified
- slim (HIV) - B20 Human immunodeficiency virus [HIV] disease
- small vessel - I73.9 Peripheral vascular disease, unspecified
- Sneddon-Wilkinson (subcorneal pustular dermatosis) - L13.1 Subcorneal pustular dermatitis
- South African creeping - B88.0 Other acariasis
- spinal (cord) - G95.9 Disease of spinal cord, unspecified
- spine - See Also: Spondylopathy;
- joint - See: Dorsopathy;
- tuberculous - A18.01 Tuberculosis of spine
- spinocerebellar (hereditary) - G11.9 Hereditary ataxia, unspecified
- specified NEC - G11.8 Other hereditary ataxias
- spleen - D73.9 Disease of spleen, unspecified
- sponge-diver's - See: Toxicity, venom, marine animal, sea anemone;
- Startle - Q89.8 Other specified congenital malformations
- Steinert's - G71.11 Myotonic muscular dystrophy
- Sticker's (erythema infectiosum) - B08.3 Erythema infectiosum [fifth disease]
- Stieda's (calcification, knee joint) - See: Bursitis, tibial collateral;
- Stokes' (exophthalmic goiter) - See: Hyperthyroidism, with, goiter (diffuse);
- Stokes-Adams (syncope with heart block) - I45.9 Conduction disorder, unspecified
- stomach - K31.9 Disease of stomach and duodenum, unspecified
- stonemason's - J62.8 Pneumoconiosis due to other dust containing silica
- storage
- glycogen - See: Disease, glycogen storage;
- mucopolysaccharide - See: Mucopolysaccharidosis;
- striatopallidal system NEC - G25.89 Other specified extrapyramidal and movement disorders
- Stuart-Prower (congenital factor X deficiency) - D68.2 Hereditary deficiency of other clotting factors
- Stuart's (congenital factor X deficiency) - D68.2 Hereditary deficiency of other clotting factors
- subcutaneous tissue - See: Disease, skin;
- supporting structures of teeth - K08.9 Disorder of teeth and supporting structures, unspecified
- specified NEC - K08.89 Other specified disorders of teeth and supporting structures
- suprarenal (capsule) (gland) - E27.9 Disorder of adrenal gland, unspecified
- sweat glands - L74.9 Eccrine sweat disorder, unspecified
- specified NEC - L74.8 Other eccrine sweat disorders
- Sweeley-Klionsky - E75.21 Fabry (-Anderson) disease
- Swift (-Feer) - See: Poisoning, mercury;
- swimming-pool granuloma - A31.1 Cutaneous mycobacterial infection
- Sylvest's (epidemic pleurodynia) - B33.0 Epidemic myalgia
- sympathetic nervous system - G90.9 Disorder of the autonomic nervous system, unspecified
- synovium - See: Disorder, synovium;
- syphilitic - See: Syphilis;
- systemic tissue mast cell - D47.02 Systemic mastocytosis
- tanapox (virus) - B08.71 Tanapox virus disease
- Tangier - E78.6 Lipoprotein deficiency
- Tarral-Besnier (pityriasis rubra pilaris) - L44.0 Pityriasis rubra pilaris
- Tauri's - E74.09 Other glycogen storage disease
- tear duct - See: Disorder, lacrimal system;
- tendon, tendinous - See Also: Disorder, tendon;
- nodular - See: Trigger finger;
- terminal vessel - I73.9 Peripheral vascular disease, unspecified
- testis - N50.9 Disorder of male genital organs, unspecified
- thalassemia Hb-S - See: Disease, sickle-cell, thalassemia;
- Thaysen-Gee (nontropical sprue) - K90.0 Celiac disease
- Thomsen - G71.12 Myotonia congenita
- throat - J39.2 Other diseases of pharynx
- septic - J02.0 Streptococcal pharyngitis
- thromboembolic - See: Embolism;
- thymus (gland) - E32.9 Disease of thymus, unspecified
- specified NEC - E32.8 Other diseases of thymus
- thyroid (gland) - E07.9 Disorder of thyroid, unspecified
- Tietze's - M94.0 Chondrocostal junction syndrome [Tietze]
- tongue - K14.9 Disease of tongue, unspecified
- specified NEC - K14.8 Other diseases of tongue
- tonsils, tonsillar (and adenoids) - J35.9 Chronic disease of tonsils and adenoids, unspecified
- tooth, teeth - K08.9 Disorder of teeth and supporting structures, unspecified
- Tourette's - F95.2 Tourette's disorder
- trachea NEC - J39.8 Other specified diseases of upper respiratory tract
- tricuspid - I07.9 Rheumatic tricuspid valve disease, unspecified
- nonrheumatic - I36.9 Nonrheumatic tricuspid valve disorder, unspecified
- triglyceride-storage - E75.5 Other lipid storage disorders
- trophoblastic - See: Mole, hydatidiform;
- tsutsugamushi - A75.3 Typhus fever due to Rickettsia tsutsugamushi
- tube (fallopian) (noninflammatory) - N83.9 Noninflammatory disorder of ovary, fallopian tube and broad ligament, unspecified
- inflammatory - See: Salpingitis;
- specified NEC - N83.8 Other noninflammatory disorders of ovary, fallopian tube and broad ligament
- tuberculous NEC - See: Tuberculosis;
- tubo-ovarian (noninflammatory) - N83.9 Noninflammatory disorder of ovary, fallopian tube and broad ligament, unspecified
- inflammatory - See: Salpingo-oophoritis;
- specified NEC - N83.8 Other noninflammatory disorders of ovary, fallopian tube and broad ligament
- tubotympanic, chronic - See: Otitis, media, suppurative, chronic, tubotympanic;
- tubulo-interstitial - N15.9 Renal tubulo-interstitial disease, unspecified
- specified NEC - N15.8 Other specified renal tubulo-interstitial diseases
- tympanum - See: Disorder, tympanic membrane;
- Uhl's - Q24.8 Other specified congenital malformations of heart
- Underwood's (sclerema neonatorum) - P83.0 Sclerema neonatorum
- Unverricht (-Lundborg) - See: Epilepsy, generalized, idiopathic;
- Urbach-Oppenheim (necrobiosis lipoidica diabeticorum) - See: E08-E13 with .620;
- ureter - N28.9 Disorder of kidney and ureter, unspecified
- in (due to)
- schistosomiasis (bilharziasis) - B65.0 Schistosomiasis due to Schistosoma haematobium [urinary schistosomiasis]
- in (due to)
- urethra - N36.9 Urethral disorder, unspecified
- specified NEC - N36.8 Other specified disorders of urethra
- urinary (tract) - N39.9 Disorder of urinary system, unspecified
- uterus (noninflammatory) - N85.9 Noninflammatory disorder of uterus, unspecified
- infective - See: Endometritis;
- inflammatory - See: Endometritis;
- specified NEC - N85.8 Other specified noninflammatory disorders of uterus
- uveal tract (anterior) - H21.9 Unspecified disorder of iris and ciliary body
- posterior - H31.9 Unspecified disorder of choroid
- vagabond's - B85.1 Pediculosis due to Pediculus humanus corporis
- vagina, vaginal (noninflammatory) - N89.9 Noninflammatory disorder of vagina, unspecified
- valve, valvular - I38 Endocarditis, valve unspecified
- van Creveld-von Gierke (glycogenosis I) - E74.01 von Gierke disease
- vas deferens - N50.9 Disorder of male genital organs, unspecified
- vascular - I99.9 Unspecified disorder of circulatory system
- arteriosclerotic - See: Arteriosclerosis;
- ciliary body NEC - See: Disorder, iris, vascular;
- hypertensive - See: Hypertension;
- iris NEC - See: Disorder, iris, vascular;
- obliterative - I77.1 Stricture of artery
- peripheral - I73.9 Peripheral vascular disease, unspecified
- occlusive - I99.8 Other disorder of circulatory system
- peripheral (occlusive) - I73.9 Peripheral vascular disease, unspecified
- in diabetes mellitus - See: E08-E13 with .51;
- vasomotor - I73.9 Peripheral vascular disease, unspecified
- vasospastic - I73.9 Peripheral vascular disease, unspecified
- vein - I87.9 Disorder of vein, unspecified
- venereal - See Also: Disease, sexually transmitted; - A64 Unspecified sexually transmitted disease
- vertebra, vertebral - See Also: Spondylopathy;
- disc - See: Disorder, disc;
- vibration - See: Vibration, adverse effects;
- vitreous - H43.9 Unspecified disorder of vitreous body
- specified NEC - H43.89 Other disorders of vitreous body
- vocal cord - J38.3 Other diseases of vocal cords
- Volkmann's, acquired - T79.6 Traumatic ischemia of muscle
- von Eulenburg's (congenital paramyotonia) - G71.19 Other specified myotonic disorders
- von Gierke's (glycogenosis I) - E74.01 von Gierke disease
- von Graefe's - See: Strabismus, paralytic, ophthalmoplegia, progressive;
- von Willebrand (-Jürgens) (angiohemophilia) - D68.00 Von Willebrand disease, unspecified
- acquired - D68.04 Acquired von Willebrand disease
- platelet-type - D68.09 Other von Willebrand disease
- pseudo - D68.09 Other von Willebrand disease
- specified NEC - D68.09 Other von Willebrand disease
- type 1 - D68.01 Von Willebrand disease, type 1
- type 1C - D68.01 Von Willebrand disease, type 1
- type 2 - D68.029 Von Willebrand disease, type 2, unspecified
- type 3 - D68.03 Von Willebrand disease, type 3
- Vrolik's (osteogenesis imperfecta) - Q78.0 Osteogenesis imperfecta
- vulva (noninflammatory) - N90.9 Noninflammatory disorder of vulva and perineum, unspecified
- Wallgren's (obstruction of splenic vein with collateral circulation) - I87.8 Other specified disorders of veins
- Wassilieff's (leptospiral jaundice) - A27.0 Leptospirosis icterohemorrhagica
- wasting NEC - E88.A Wasting disease (syndrome) due to underlying condition
- Waterhouse-Friderichsen - A39.1 Waterhouse-Friderichsen syndrome
- Wegner's (syphilitic osteochondritis) - A50.02 Early congenital syphilitic osteochondropathy
- Weil's (leptospiral jaundice of lung) - A27.0 Leptospirosis icterohemorrhagica
- Weir Mitchell's (erythromelalgia) - I73.81 Erythromelalgia
- Werdnig-Hoffmann - G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
- Wermer's - E31.21 Multiple endocrine neoplasia [MEN] type I
- Werner-His (trench fever) - A79.0 Trench fever
- Werner-Schultz (neutropenic splenomegaly) - D73.81 Neutropenic splenomegaly
- Wernicke-Posadas - B38.9 Coccidioidomycosis, unspecified
- whipworm - B79 Trichuriasis
- white blood cells - D72.9 Disorder of white blood cells, unspecified
- specified NEC - D72.89 Other specified disorders of white blood cells
- white matter - R90.82 White matter disease, unspecified
- white-spot, meaning lichen sclerosus et atrophicus - L90.0 Lichen sclerosus et atrophicus
- Wilkie's - K55.1 Chronic vascular disorders of intestine
- Wilkinson-Sneddon (subcorneal pustular dermatosis) - L13.1 Subcorneal pustular dermatitis
- Willis' - See: Diabetes;
- Wilson's (hepatolenticular degeneration) - E83.01 Wilson's disease
- woolsorter's - A22.1 Pulmonary anthrax
- yaba monkey tumor - B08.72 Yaba pox virus disease
- yaba pox (virus) - B08.72 Yaba pox virus disease
- Zika virus - A92.5 Zika virus disease
- congenital - P35.4 Congenital Zika virus disease
- zoonotic, bacterial - A28.9 Zoonotic bacterial disease, unspecified
- specified type NEC - A28.8 Other specified zoonotic bacterial diseases, not elsewhere classified
Applicable Clinical Terms Definitions
Altitude: A vertical distance measured from a known level on the surface of a planet or other celestial body.
Amyloid: A fibrous protein complex that consists of proteins folded into a specific cross beta-pleated sheet structure. This fibrillar structure has been found as an alternative folding pattern for a variety of functional proteins. Deposits of amyloid in the form of AMYLOID PLAQUES are associated with a variety of degenerative diseases. The amyloid structure has also been found in a number of functional proteins that are unrelated to disease.
Appendix: A worm-like blind tube extension from the CECUM.
Arteries: The vessels carrying blood away from the heart.
Basal Ganglia: Large subcortical nuclear masses derived from the telencephalon and located in the basal regions of the cerebral hemispheres.
Blood: The body fluid that circulates in the vascular system (BLOOD VESSELS). Whole blood includes PLASMA and BLOOD CELLS.
Bone and Bones: A specialized CONNECTIVE TISSUE that is the main constituent of the SKELETON. The principal cellular component of bone is comprised of OSTEOBLASTS; OSTEOCYTES; and OSTEOCLASTS, while FIBRILLAR COLLAGENS and hydroxyapatite crystals form the BONE MATRIX.
Brain: The part of CENTRAL NERVOUS SYSTEM that is contained within the skull (CRANIUM). Arising from the NEURAL TUBE, the embryonic brain is comprised of three major parts including PROSENCEPHALON (the forebrain); MESENCEPHALON (the midbrain); and RHOMBENCEPHALON (the hindbrain). The developed brain consists of CEREBRUM; CEREBELLUM; and other structures in the BRAIN STEM.
Breast: In humans, one of the paired regions in the anterior portion of the THORAX. The breasts consist of the MAMMARY GLANDS, the SKIN, the MUSCLES, the ADIPOSE TISSUE, and the CONNECTIVE TISSUES.
California: State bounded on the east by Nevada and Arizona, on the south by Mexico and the Pacific Ocean on the south and west, and on the north by Oregon.
Capillaries: The minute vessels that connect arterioles and venules.
Cartilage: A non-vascular form of connective tissue composed of CHONDROCYTES embedded in a matrix that includes CHONDROITIN SULFATE and various types of FIBRILLAR COLLAGEN. There are three major types: HYALINE CARTILAGE; FIBROCARTILAGE; and ELASTIC CARTILAGE.
Cecum: The blind sac or outpouching area of the LARGE INTESTINE that is below the entrance of the SMALL INTESTINE. It has a worm-like extension, the vermiform APPENDIX.
Chicago: A city in Illinois.
Choroid: The thin, highly vascular membrane covering most of the posterior of the eye between the RETINA and SCLERA.
Ciliary Body: A ring of tissue extending from the scleral spur to the ora serrata of the RETINA. It consists of the uveal portion and the epithelial portion. The ciliary muscle is in the uveal portion and the ciliary processes are in the epithelial portion.
Colon: The segment of LARGE INTESTINE between the CECUM and the RECTUM. It includes the ASCENDING COLON; the TRANSVERSE COLON; the DESCENDING COLON; and the SIGMOID COLON.
Conjunctiva: The mucous membrane that covers the posterior surface of the eyelids and the anterior pericorneal surface of the eyeball.
Cornea: The transparent anterior portion of the fibrous coat of the eye consisting of five layers: stratified squamous CORNEAL EPITHELIUM; BOWMAN MEMBRANE; CORNEAL STROMA; DESCEMET MEMBRANE; and mesenchymal CORNEAL ENDOTHELIUM. It serves as the first refracting medium of the eye. It is structurally continuous with the SCLERA, avascular, receiving its nourishment by permeation through spaces between the lamellae, and is innervated by the ophthalmic division of the TRIGEMINAL NERVE via the ciliary nerves and those of the surrounding conjunctiva which together form plexuses. (Cline et al., Dictionary of Visual Science, 4th ed)
COVID-19: A viral disorder generally characterized by high FEVER; COUGH; DYSPNEA; CHILLS; PERSISTENT TREMOR; MUSCLE PAIN; HEADACHE; SORE THROAT; a new loss of taste and/or smell (see AGEUSIA and ANOSMIA) and other symptoms of a VIRAL PNEUMONIA. In severe cases, a myriad of coagulopathy associated symptoms often correlating with COVID-19 severity is seen (e.g., BLOOD COAGULATION; THROMBOSIS; ACUTE RESPIRATORY DISTRESS SYNDROME; SEIZURES; HEART ATTACK; STROKE; multiple CEREBRAL INFARCTIONS; KIDNEY FAILURE; catastrophic ANTIPHOSPHOLIPID ANTIBODY SYNDROME and/or DISSEMINATED INTRAVASCULAR COAGULATION). In younger patients, rare inflammatory syndromes are sometimes associated with COVID-19 (e.g., atypical KAWASAKI SYNDROME; TOXIC SHOCK SYNDROME; pediatric multisystem inflammatory disease; and CYTOKINE STORM SYNDROME). A coronavirus, SARS-CoV-2, in the genus BETACORONAVIRUS is the causative agent.
Diaphragm: The musculofibrous partition that separates the THORACIC CAVITY from the ABDOMINAL CAVITY. Contraction of the diaphragm increases the volume of the thoracic cavity aiding INHALATION.
Digestive System: A group of organs stretching from the MOUTH to the ANUS, serving to breakdown foods, assimilate nutrients, and eliminate waste. In humans, the digestive system includes the GASTROINTESTINAL TRACT and the accessory glands (LIVER; BILIARY TRACT; PANCREAS).
Duodenum: The shortest and widest portion of the SMALL INTESTINE adjacent to the PYLORUS of the STOMACH. It is named for having the length equal to about the width of 12 fingers.
Ear: The hearing and equilibrium system of the body. It consists of three parts: the EXTERNAL EAR, the MIDDLE EAR, and the INNER EAR. Sound waves are transmitted through this organ where vibration is transduced to nerve signals that pass through the ACOUSTIC NERVE to the CENTRAL NERVOUS SYSTEM. The inner ear also contains the vestibular organ that maintains equilibrium by transducing signals to the VESTIBULAR NERVE.
Echinococcus: A genus of very small TAPEWORMS, in the family Taeniidae. The adult form is found in various CARNIVORA but not humans. The larval form is seen in humans under certain epidemiologic circumstances.
Epididymis: The convoluted cordlike structure attached to the posterior of the TESTIS. Epididymis consists of the head (caput), the body (corpus), and the tail (cauda). A network of ducts leaving the testis joins into a common epididymal tubule proper which provides the transport, storage, and maturation of SPERMATOZOA.
Esophagus: The muscular membranous segment between the PHARYNX and the STOMACH in the UPPER GASTROINTESTINAL TRACT.
Eustachian Tube: A narrow passageway that connects the upper part of the throat to the TYMPANIC CAVITY.
Eye: The organ of sight constituting a pair of globular organs made up of a three-layered roughly spherical structure specialized for receiving and responding to light.
Eyelids: Each of the upper and lower folds of SKIN which cover the EYE when closed.
Frontal Sinus: One of the paired, but seldom symmetrical, air spaces located between the inner and outer compact layers of the FRONTAL BONE in the forehead.
Gallbladder: A storage reservoir for BILE secretion. Gallbladder allows the delivery of bile acids at a high concentration and in a controlled manner, via the CYSTIC DUCT to the DUODENUM, for degradation of dietary lipid.
Gingiva: Oral tissue surrounding and attached to TEETH.
Gingiva: Oral tissue surrounding and attached to TEETH.
Ancylostomatoidea: A superfamily of nematode parasitic hookworms consisting of four genera: ANCYLOSTOMA; NECATOR; Bunostomum; and Uncinaria. ANCYLOSTOMA and NECATOR occur in humans and other mammals. Bunostomum is common in ruminants and Uncinaria in wolves, foxes, and dogs.
Iceland: A country in northern Europe, an island between the Greenland Sea and the North Atlantic Ocean, northwest of the United Kingdom. The capital is Reykjavik.
Intervertebral Disc: Any of the 23 plates of fibrocartilage found between the bodies of adjacent VERTEBRAE.
Intestines: The section of the alimentary canal from the STOMACH to the ANAL CANAL. It includes the LARGE INTESTINE and SMALL INTESTINE.
Iris: The most anterior portion of the uveal layer, separating the anterior chamber from the posterior. It consists of two layers - the stroma and the pigmented epithelium. Color of the iris depends on the amount of melanin in the stroma on reflection from the pigmented epithelium.
Jaw: Bony structure of the mouth that holds the teeth. It consists of the MANDIBLE and the MAXILLA.
Joints: Also known as articulations, these are points of connection between the ends of certain separate bones, or where the borders of other bones are juxtaposed.
Kuru: A prion disease found exclusively among the Fore linguistic group natives of the highlands of NEW GUINEA. The illness is primarily restricted to adult females and children of both sexes. It is marked by the subacute onset of tremor and ataxia followed by motor weakness and incontinence. Death occurs within 3-6 months of disease onset. The condition is associated with ritual cannibalism, and has become rare since this practice has been discontinued. Pathologic features include a noninflammatory loss of neurons that is most prominent in the cerebellum, glial proliferation, and amyloid plaques. (From Adams et al., Principles of Neurology, 6th ed, p773)
Larynx: A tubular organ of VOICE production. It is located in the anterior neck, superior to the TRACHEA and inferior to the tongue and HYOID BONE.
Lip: Either of the two fleshy, full-blooded margins of the mouth.
Lumbosacral Region: Region of the back including the LUMBAR VERTEBRAE, SACRUM, and nearby structures.
Lung: Either of the pair of organs occupying the cavity of the thorax that effect the aeration of the blood.
Mediastinum: A membrane in the midline of the THORAX of mammals. It separates the lungs between the STERNUM in front and the VERTEBRAL COLUMN behind. It also surrounds the HEART, TRACHEA, ESOPHAGUS, THYMUS, and LYMPH NODES.
Ear, Middle: The space and structures directly internal to the TYMPANIC MEMBRANE and external to the inner ear (LABYRINTH). Its major components include the AUDITORY OSSICLES and the EUSTACHIAN TUBE that connects the cavity of middle ear (tympanic cavity) to the upper part of the throat.
Muscles: Contractile tissue that produces movement in animals.
Nails: The thin, horny plates that cover the dorsal surfaces of the distal phalanges of the fingers and toes of primates.
Nervous System: The entire nerve apparatus, composed of a central part, the brain and spinal cord, and a peripheral part, the cranial and spinal nerves, autonomic ganglia, and plexuses. (Stedman, 26th ed)
Nipples: The conic organs which usually give outlet to milk from the mammary glands.
Nose: A part of the upper respiratory tract. It contains the organ of SMELL. The term includes the external nose, the nasal cavity, and the PARANASAL SINUSES.
Nucleus Pulposus: Fibrocartilage inner core of the intervertebral disc. Prolapsed or bulged nucleus pulposus leads to INTERVERTEBRAL DISC DISPLACEMENT while proliferation of cells in the nucleus pulposus is associated with INTERVERTEBRAL DISC DEGENERATION.
Orbit: Bony cavity that holds the eyeball and its associated tissues and appendages.
Ear, External: The outer part of the hearing system of the body. It includes the shell-like EAR AURICLE which collects sound, and the EXTERNAL EAR CANAL, the TYMPANIC MEMBRANE, and the EXTERNAL EAR CARTILAGES.
Pancreas: A nodular organ in the ABDOMEN that contains a mixture of ENDOCRINE GLANDS and EXOCRINE GLANDS. The small endocrine portion consists of the ISLETS OF LANGERHANS secreting a number of hormones into the blood stream. The large exocrine portion (EXOCRINE PANCREAS) is a compound acinar gland that secretes several digestive enzymes into the pancreatic ductal system that empties into the DUODENUM.
Penis: The external reproductive organ of males. It is composed of a mass of erectile tissue enclosed in three cylindrical fibrous compartments. Two of the three compartments, the corpus cavernosa, are placed side-by-side along the upper part of the organ. The third compartment below, the corpus spongiosum, houses the urethra.
Periosteum: Thin outer membrane that surrounds a bone. It contains CONNECTIVE TISSUE, CAPILLARIES, nerves, and a number of cell types.
Peritoneum: A membrane of squamous EPITHELIAL CELLS, the mesothelial cells, covered by apical MICROVILLI that allow rapid absorption of fluid and particles in the PERITONEAL CAVITY. The peritoneum is divided into parietal and visceral components. The parietal peritoneum covers the inside of the ABDOMINAL WALL. The visceral peritoneum covers the intraperitoneal organs. The double-layered peritoneum forms the MESENTERY that suspends these organs from the abdominal wall.
Pharynx: A funnel-shaped fibromuscular tube that conducts food to the ESOPHAGUS, and air to the LARYNX and LUNGS. It is located posterior to the NASAL CAVITY; ORAL CAVITY; and LARYNX, and extends from the SKULL BASE to the inferior border of the CRICOID CARTILAGE anteriorly and to the inferior border of the C6 vertebra posteriorly. It is divided into the NASOPHARYNX; OROPHARYNX; and HYPOPHARYNX (laryngopharynx).
Pineal Gland: A light-sensitive neuroendocrine organ attached to the roof of the THIRD VENTRICLE of the brain. The pineal gland secretes MELATONIN, other BIOGENIC AMINES and NEUROPEPTIDES.
Polyethylene: A vinyl polymer made from ethylene. It can be branched or linear. Branched or low-density polyethylene is tough and pliable but not to the same degree as linear polyethylene. Linear or high-density polyethylene has a greater hardness and tensile strength. Polyethylene is used in a variety of products, including implants and prostheses.
Prostate: A gland in males that surrounds the neck of the URINARY BLADDER and the URETHRA. It secretes a substance that liquefies coagulated semen. It is situated in the pelvic cavity behind the lower part of the PUBIC SYMPHYSIS, above the deep layer of the triangular ligament, and rests upon the RECTUM.
Rectum: The distal segment of the LARGE INTESTINE, between the SIGMOID COLON and the ANAL CANAL.
Sclera: The white, opaque, fibrous, outer tunic of the eyeball, covering it entirely excepting the segment covered anteriorly by the cornea. It is essentially avascular but contains apertures for vessels, lymphatics, and nerves. It receives the tendons of insertion of the extraocular muscles and at the corneoscleral junction contains the CANAL OF SCHLEMM. (From Cline et al., Dictionary of Visual Science, 4th ed)
Scrotum: A cutaneous pouch of skin containing the testicles and spermatic cords.
Sebaceous Glands: Small, sacculated organs found within the DERMIS. Each gland has a single duct that emerges from a cluster of oval alveoli. Each alveolus consists of a transparent BASEMENT MEMBRANE enclosing epithelial cells. The ducts from most sebaceous glands open into a HAIR FOLLICLE, but some open on the general surface of the SKIN. Sebaceous glands secrete SEBUM.
Seminal Vesicles: A saclike, glandular diverticulum on each ductus deferens in male vertebrates. It is united with the excretory duct and serves for temporary storage of semen. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)
Sin Nombre virus: A species of ORTHOHANTAVIRUS which emerged in the Four Corners area of the United States in 1993. It causes a serious, often fatal pulmonary illness (HANTAVIRUS PULMONARY SYNDROME) in humans. Transmission is by inhaling aerosolized rodent secretions that contain virus particles, carried especially by deer mice (PEROMYSCUS maniculatus) and pinyon mice (P. truei).
Skin: The outer covering of the body that protects it from the environment. It is composed of the DERMIS and the EPIDERMIS.
Spine: The spinal or vertebral column.
Spleen: An encapsulated lymphatic organ through which venous blood filters.
Stomach: An organ of digestion situated in the left upper quadrant of the abdomen between the termination of the ESOPHAGUS and the beginning of the DUODENUM.
Subcutaneous Tissue: Loose connective tissue lying under the DERMIS, which binds SKIN loosely to subjacent tissues. It may contain a pad of ADIPOCYTES, which vary in number according to the area of the body and vary in size according to the nutritional state.
Sweat Glands: Sweat-producing structures that are embedded in the DERMIS. Each gland consists of a single tube, a coiled body, and a superficial duct.
Sympathetic Nervous System: The thoracolumbar division of the autonomic nervous system. Sympathetic preganglionic fibers originate in neurons of the intermediolateral column of the spinal cord and project to the paravertebral and prevertebral ganglia, which in turn project to target organs. The sympathetic nervous system mediates the body's response to stressful situations, i.e., the fight or flight reactions. It often acts reciprocally to the parasympathetic system.
Testis: The male gonad containing two functional parts: the SEMINIFEROUS TUBULES for the production and transport of male germ cells (SPERMATOGENESIS) and the interstitial compartment containing LEYDIG CELLS that produce ANDROGENS.
Tongue: A muscular organ in the mouth that is covered with pink tissue called mucosa, tiny bumps called papillae, and thousands of taste buds. The tongue is anchored to the mouth and is vital for chewing, swallowing, and for speech.
Ureter: One of a pair of thick-walled tubes that transports urine from the KIDNEY PELVIS to the URINARY BLADDER.
Urethra: A tube that transports URINE from the URINARY BLADDER to the outside of the body in both the sexes. It also has a reproductive function in the male by providing a passage for SPERM.
Vas Deferens: The excretory duct of the testes that carries SPERMATOZOA. It rises from the SCROTUM and joins the SEMINAL VESICLES to form the ejaculatory duct.
Veins: The vessels carrying blood away from the CAPILLARY BEDS.
Vibration: A continuing periodic change in displacement with respect to a fixed reference. (McGraw-Hill Dictionary of Scientific and Technical Terms, 6th ed)
Vocal Cords: A pair of cone-shaped elastic mucous membrane projecting from the laryngeal wall and forming a narrow slit between them. Each contains a thickened free edge (vocal ligament) extending from the THYROID CARTILAGE to the ARYTENOID CARTILAGE, and a VOCAL MUSCLE that shortens or relaxes the vocal cord to control sound production.
White Matter: The region of CENTRAL NERVOUS SYSTEM that appears lighter in color than the other type, GRAY MATTER. It mainly consists of MYELINATED NERVE FIBERS and contains few neuronal cell bodies or DENDRITES.
Zika Virus: An arbovirus in the FLAVIVIRUS genus of the family FLAVIVIRIDAE. Originally isolated in the Zika Forest of UGANDA it has been introduced to Asia and the Americas.
