Disease, diseased - in the ICD-10-CM Index
Annotation Back-References in the 2025 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
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
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
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
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
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
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
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;
lumbar (with)
lumbosacral (with)
specified NEC - See: Disorder, disc, specified NEC;
thoracic (with)
thoracolumbar (with)
with myelopathy - See: Disorder, disc, with, myelopathy;
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
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
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
veno-occlusive - K76.5 Hepatic veno-occlusive disease
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
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
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
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
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
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
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
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
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
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
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
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;
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
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
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
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
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
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
without crisis - D57.44 Sickle-cell thalassemia beta plus without crisis
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
without crisis - D57.42 Sickle-cell thalassemia beta zero without crisis
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
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]
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.
