Disease, diseased
"Disease, diseased" References in the ICD-10-CM Index to Diseases and Injuries
References in the ICD-10-CM Index to Diseases and Injuries 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;
- 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
- 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 - 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 - 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
- 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's - 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
- 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 (congenital pancytopenia) - D61.09 Other constitutional aplastic 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
- 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 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 - I25.89 Other forms of chronic ischemic heart disease
- 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
- splenic sequestration - D57.452 Sickle-cell thalassemia beta plus with splenic sequestration
- vasoocclusive pain - D57.459 Sickle-cell thalassemia beta plus with crisis, unspecified
- 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
- splenic sequestration - D57.432 Sickle-cell thalassemia beta zero with splenic sequestration
- vasoocclusive pain - D57.439 Sickle-cell thalassemia beta zero with crisis, unspecified
- 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
- splenic sequestration - D57.02 Hb-SS disease with splenic sequestration
- vasoocclusive pain - D57.00 Hb-SS disease with crisis, unspecified
- 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
- 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's - See: Epilepsy, generalized, idiopathic;
- 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
- of childhood, specified NEC - J84.848 Other interstitial lung diseases of childhood
- 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 - J44.9 Chronic obstructive pulmonary disease, unspecified
- bronchiectasis - J47.9 Bronchiectasis, uncomplicated
- bronchitis - J44.9 Chronic obstructive pulmonary disease, unspecified
- 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
- 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
- myelodysplastic - See Also: Syndrome, myelodysplasia; - 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 Parkinson's disease
- 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
- 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
- with specified complication NEC - 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
- vasoocclusive pain - D57.219 Sickle-cell/Hb-C disease with crisis, unspecified
- 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
- with complication specified NEC - D57.818 Other sickle-cell disorders with crisis with other specified complication
- splenic sequestration - D57.812 Other sickle-cell disorders with splenic sequestration
- vasoocclusive pain - D57.819 Other sickle-cell disorders with crisis, unspecified
- 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
- with complication specified NEC - D57.818 Other sickle-cell disorders with crisis with other specified complication
- splenic sequestration - D57.812 Other sickle-cell disorders with splenic sequestration
- vasoocclusive pain - D57.819 Other sickle-cell disorders with crisis, unspecified
- 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
- with complication specified NEC - D57.818 Other sickle-cell disorders with crisis with other specified complication
- splenic sequestration - D57.812 Other sickle-cell disorders with splenic sequestration
- vasoocclusive pain - D57.819 Other sickle-cell disorders with crisis, unspecified
- 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
- splenic sequestration - D57.812 Other sickle-cell disorders with splenic sequestration
- vasoocclusive pain - D57.819 Other sickle-cell disorders with crisis, unspecified
- 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
- 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
- splenic sequestration - D57.452 Sickle-cell thalassemia beta plus with splenic sequestration
- vasoocclusive pain - D57.459 Sickle-cell thalassemia beta plus with crisis, unspecified
- 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
- splenic sequestration - D57.432 Sickle-cell thalassemia beta zero with splenic sequestration
- vasoocclusive pain - D57.439 Sickle-cell thalassemia beta zero with crisis, unspecified
- 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
- splenic sequestration - D57.412 Sickle-cell thalassemia, unspecified, with splenic sequestration
- vasoocclusive pain - D57.419 Sickle-cell thalassemia, unspecified, with crisis
- 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
- with complication specified NEC - D57.09 Hb-SS disease with crisis with other specified complication
- splenic sequestration - D57.02 Hb-SS disease with splenic sequestration
- vasoocclusive pain - D57.00 Hb-SS disease with crisis, unspecified
- 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 - R64 Cachexia
- 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
