ICD-10-CM Alphabetic Index to Diseases and Injuries

Syndrome

Follow the subterms below to reach a more specific code.

— see also Disease

4H G11.5
5q minus NOS D46.C
22q13.3 deletion Q93.52
48,XXXX Q97.1
49,XXXXX Q97.1
abdominal
acute R10.0
muscle deficiency Q79.4
abnormal innervation H02.519
left H02.516
lower H02.515
upper H02.514
right H02.513
lower H02.512
upper H02.511
abstinence, neonatal P96.1
acid pulmonary aspiration, obstetric O74.0
acquired immunodeficiency — see Human, immunodeficiency virus (HIV) disease
activated phosphoinositide 3-kinase delta syndrome [APDS] D81.82
acute abdominal R10.0
acute respiratory distress (adult) (child) J80
idiopathic J84.114
Adair-Dighton Q78.0
Adams-Stokes (-Morgagni) I45.9
adiposogenital E23.6
adrenal
hemorrhage (meningococcal) A39.1
meningococcic A39.1
adrenocortical — see Cushing's, syndrome
adrenogenital E25.9
congenital, associated with enzyme deficiency E25.0
afferent loop NEC K91.89
Aicardi-Goutières E79.81
Alagille (-Watson) Q44.71
alcohol withdrawal (without convulsions) — see Dependence, alcohol, with, withdrawal
Alder's D72.0
Aldrich (-Wiskott) D82.0
alien hand R41.4
Alpha-gal Z91.014
Alport Q87.81
alveolar hypoventilation E66.2
alveolocapillary block J84.10
amnesic, amnestic (confabulatory) (due to) — see Disorder, amnesic
amyostatic (Wilson's disease) E83.01
androgen insensitivity E34.50
complete E34.51
partial E34.52
androgen resistance E34.50 — see also Syndrome, androgen insensitivity
Angelman Q93.51
anginal — see Angina
ankyloglossia superior Q38.1
anterior
chest wall R07.89
cord G83.82
spinal artery G95.19
compression M47.019
cervical region M47.012
cervicothoracic region M47.013
lumbar region M47.016
occipito-atlanto-axial region M47.011
thoracic region M47.014
thoracolumbar region M47.015
tibial M76.81-
antibody deficiency D80.9
agammaglobulinemic D80.1
hereditary D80.0
congenital D80.0
hypogammaglobulinemic D80.1
hereditary D80.0
anticardiolipin (-antibody) D68.61
antidepressant discontinuation T43.205
antiphospholipid (-antibody) D68.61
aortic
arch M31.4
bifurcation I74.09
aortomesenteric duodenum occlusion K31.5
apical ballooning (transient left ventricular) I51.81
arcuate ligament I77.4
argentaffin, argintaffinoma E34.09
Arnold-Chiari — see Arnold-Chiari disease
Arrillaga-Ayerza I27.0
arterial tortuosity Q87.82
arteriovenous steal T82.898-
Asherman's N85.6
aspiration, of newborn — see Aspiration, by substance, with pneumonia
meconium P24.01
ataxia-telangiectasia G11.3
auriculotemporal G50.8
autoerythrocyte sensitization (Gardner-Diamond) D69.2
autoimmune polyglandular E31.0
autoimmune lymphoproliferative [ALPS] D89.82
autoinflammatory M04.9
specified type NEC M04.8
autosomal — see Abnormal, autosomes
Avellis' G46.8
Axenfeld-Rieger Q13.81
Ayerza (-Arrillaga) I27.0
Babinski-Nageotte G83.89
Bakwin-Krida Q78.5
Bardet-Biedl Q87.83
bare lymphocyte D81.6
Barré-Guillain G61.0
Barré-Liéou M53.0
Barrett's — see Barrett's, esophagus
Barsony-Polgar K22.4
Barsony-Teschendorf K22.4
Barth E78.71
Bartter's E26.81
basal cell nevus Q87.89
Basedow's E05.00
with thyroid storm E05.01
basilar artery G45.0
Batten-Steinert G71.11
battered
baby or child — see Maltreatment, child, physical abuse
spouse — see Maltreatment, adult, physical abuse
Beals Q87.40
Beau's I51.5
Beck's I65.8
Benedikt's G46.3
Béquez César (-Steinbrinck-Chédiak-Higashi) E70.330
Berardinelli-Siep E88.12
Bernhardt-Roth — see Meralgia paresthetica
Bernheim's — see Failure, heart, right
big spleen D73.1
bilateral polycystic ovarian E28.2
Bing-Horton's — see Horton's headache
Birt-Hogg-Dube syndrome Q87.89
Björck (-Thorsen) E34.09
black
lung J60
widow spider bite — see Toxicity, venom, spider, black widow
Blackfan-Diamond D61.01
Blau M04.8
blind loop K90.2
congenital Q43.8
postsurgical K91.2
blue sclera Q78.0
blue toe I75.02-
Boder-Sedgewick G11.3
Boerhaave's K22.3
Borjeson Forssman Lehmann Q89.89
Bouillaud's I01.9
Bourneville (-Pringle) Q85.1
Bouveret (-Hoffman) I47.9
brachial plexus G54.0
bradycardia-tachycardia I49.5
brain (nonpsychotic) F09
with psychosis, psychotic reaction F09
acute or subacute — see Delirium
congenital — see Disability, intellectual
organic F09
post-traumatic (nonpsychotic) F07.81
psychotic F09
personality change F07.0
postcontusional F07.81
post-traumatic, nonpsychotic F07.81
psycho-organic F09
psychotic F06.8
brain stem stroke G46.3
Brandt's (acrodermatitis enteropathica) E83.2
BRCA1-cancer predisposition QA1.790
BRCA2-cancer predisposition QA1.791
broad ligament laceration N83.8
Brock's J98.11
bronchiolitis obliterans J44.81 — see also Bronchiolitis, obliterative
bronze baby P83.88
Brown-Sequard G83.81
Brugada I49.81
bubbly lung P27.0
Buchem's M85.2
Budd-Chiari I82.0
bulbar (progressive) G12.22
Bürger-Grütz E78.3
Burke's K86.89
Burnett's (milk-alkali) E83.52
burning feet E53.9
Bywaters' T79.5
Call-Fleming I67.841
cannabinoid hyperemesis R11.16
cannabis hyperemesis R11.16
carbohydrate-deficient glycoprotein (CDGS) E77.8
carcinogenic thrombophlebitis I82.1
carcinoid E34.00
heart E34.01
specified NEC E34.09
cardiac asthma I50.1
cardiacos negros I27.0
cardiofaciocutaneous Q87.89
cardiopulmonary-obesity E66.2
cardiorenal Note: — see Failure, heart; also see Failure, renal
cardiorespiratory distress (idiopathic), newborn P22.0
cardiovascular renal Note: — see Failure, heart; also see Failure, renal
carotid
artery (hemispheric) (internal) G45.1
body G90.01
sinus G90.01
carpal tunnel G56.0-
Cassidy (-Scholte) E34.09
cat cry Q93.4
cat eye Q92.8
cauda equina G83.4
causalgia — see Causalgia
celiac K90.0
artery compression I77.4
axis I77.4
central pain G89.0
cerebellar
hereditary G11.9
stroke G46.4
cerebellomedullary malformation — see Spina bifida
cerebral
artery
anterior G46.1
middle G46.0
posterior G46.2
gigantism E22.0
cervical (root) M53.1
disc — see Disorder, disc, cervical, with neuritis
fusion Q76.1
posterior, sympathicus M53.0
rib Q76.5
sympathetic paralysis G90.2
cervicobrachial (diffuse) M53.1
cervicocranial M53.0
cervicodorsal outlet G54.2
cervicothoracic outlet G54.0 — see also Syndrome, thoracic outlet
Céstan (-Raymond) I65.8
Charcot's (angina cruris) (intermittent claudication) I73.9
Charcot-Weiss-Baker G90.09
CHARGE Q89.89
Chédiak-Higashi (-Steinbrinck) E70.330
chest wall R07.1
Chiari's (hepatic vein thrombosis) I82.0
Chilaiditi's Q43.3
child maltreatment — see Maltreatment, child
chondrocostal junction M94.0
chondroectodermal dysplasia Q77.6
chromosome 4 short arm deletion Q93.3
chromosome 5 short arm deletion Q93.4
chronic
infantile neurological, cutaneous and articular (CINCA) M04.2
pain G89.4
personality F68.8
Churg-Strauss M30.1
Clarke-Hadfield K86.89
Clerambault's automatism G93.89
clinically isolated G37.9
Clouston's (hidrotic ectodermal dysplasia) Q82.4
clumsiness, clumsy child F82
cluster headache G44.009
intractable G44.001
not intractable G44.009
Coffin-Lowry Q89.89
cold injury (newborn) P80.0
combined immunity deficiency D81.9
compartment (deep) (posterior) (traumatic) T79.A0
abdomen T79.A3
lower extremity (hip, buttock, thigh, leg, foot, toes) T79.A2
nontraumatic
abdomen M79.A3
lower extremity (hip, buttock, thigh, leg, foot, toes) M79.A2-
specified site NEC M79.A9
upper extremity (shoulder, arm, forearm, wrist, hand, fingers) M79.A1-
postprocedural — see Syndrome, compartment, nontraumatic
specified site NEC T79.A9
upper extremity (shoulder, arm, forearm, wrist, hand, fingers) T79.A1
complex regional pain — see Syndrome, pain, complex regional
compression T79.5
anterior spinal — see Syndrome, anterior, spinal artery, compression
cauda equina G83.4
celiac artery I77.4
vertebral artery M47.029
occipito-atlanto-axial region M47.021
cervical region M47.022
concussion F07.81
congenital
affecting multiple systems NEC Q87.89
central alveolar hypoventilation G47.35
facial diplegia Q87.0
muscular hypertrophy-cerebral Q87.89
oculo-auriculovertebral Q87.0
oculofacial diplegia (Moebius) Q87.0
rubella (manifest) P35.0
congestion-fibrosis (pelvic), female N94.89
congestive dysmenorrhea N94.6
Conn's E26.01
connective tissue M35.9
overlap NEC M35.1
conus medullaris G95.81
cord
anterior G83.82
posterior G83.83
coronary
acute NEC I24.9
insufficiency or intermediate I20.0
slow flow I20.89
Costen's (complex) M26.69
costochondral junction M94.0
costoclavicular G54.0
costovertebral E22.0
Cowden
PTEN related Q85.81
specified NEC Q85.82
craniovertebral M53.0
Creutzfeldt-Jakob — see Creutzfeldt-Jakob disease or syndrome
cri-du-chat Q93.4
crib death R99
cricopharyngeal — see Dysphagia
croup J05.0
CRPS I — see Syndrome, pain, complex regional I
crush T79.5
CTNNB1 Q87.88
cubital tunnel — see Lesion, nerve, ulnar
Curschmann (-Batten) (-Steinert) G71.11
Cushing's E24.9
alcohol-induced E24.4
due to
alcohol
drugs E24.2
ectopic ACTH E24.3
overproduction of pituitary ACTH E24.0
drug-induced E24.2
overdose or wrong substance given or taken — see Table of Drugs and Chemicals, by drug, poisoning
pituitary-dependent E24.0
specified type NEC E24.8
cryopyrin-associated periodic M04.2
cryptophthalmos Q87.0
cystic duct stump K91.5
cytokine release D89.839
grade 1 D89.831
grade 2 D89.832
grade 3 D89.833
grade 4 D89.834
grade 5 D89.835
Dana-Putnam D51.0
Danbolt (-Cross) (acrodermatitis enteropathica) E83.2
Dandy-Walker Q03.1
with spina bifida Q07.01
Danlos' Q79.60 — see also Syndrome, Ehlers-Danlos
defibrination — see also Fibrinolysis
with
antepartum hemorrhage — see Hemorrhage, antepartum, with coagulation defect
intrapartum hemorrhage — see Hemorrhage, complicating, delivery
newborn P60
postpartum O72.3
Degos' I77.89
Déjérine-Roussy G89.0
delayed sleep phase G47.21
demyelinating G37.9
dependence — see F10-F19 with fourth character .2
depersonalization (-derealization) F48.1
De Quervain E34.51
de Toni-Fanconi (-Debré) E72.09
with cystinosis E72.04
de Vivo syndrome E74.810
diabetes mellitus-hypertension-nephrosis — see Diabetes, nephrosis
diabetes mellitus in newborn infant P70.2
diabetes-nephrosis — see Diabetes, nephrosis
diabetic amyotrophy — see Diabetes, amyotrophy
dialysis associated steal T82.898-
Diamond-Blackfan D61.01
Diamond-Gardener D69.2
DIC (diffuse or disseminated intravascular coagulopathy) D65
di George's D82.1
Dighton's Q78.0
disequilibrium E87.8
Döhle body-panmyelopathic D72.0
dorsolateral medullary G46.4
double athetosis G80.3
Down Q90.9 — see also Down syndrome
Dravet (intractable) G40.834
with status epilepticus G40.833
without status epilepticus G40.834
Dresbach's (elliptocytosis) D58.1
DRESS (drug rash with eosinophilia and systemic symptoms) D72.12
Dressler's (postmyocardial infarction) I24.1
postcardiotomy I97.0
drug rash with eosinophilia and systemic symptoms (DRESS) D72.12
drug withdrawal, infant of dependent mother P96.1
dry eye H04.12-
due to abnormality
chromosomal Q99.9
sex
female phenotype Q97.9
male phenotype Q98.9
specified NEC Q99.8
dumping (postgastrectomy) K91.1
nonsurgical K31.89
Dupré's (meningism) R29.1
dysmetabolic X E88.810
dyspraxia, developmental F82
Eagle-Barrett Q79.4
Eaton-Lambert — see Syndrome, Lambert-Eaton
Ebstein's Q22.5
ectopic ACTH E24.3
eczema-thrombocytopenia D82.0
Eddowes' Q78.0
effort (psychogenic) F45.8
Eisenmenger's I27.83
Ehlers-Danlos Q79.60
classical (cEDS) (classical EDS) Q79.61
hypermobile (hEDS) (hypermobile EDS) Q79.62
specified NEC Q79.69
vascular (vascular EDS) (vEDS) Q79.63
Ekman's Q78.0
electric feet E53.8
Ellis-van Creveld Q77.6
empty nest Z60.0
endocrine-hypertensive E27.0
entrapment — see Neuropathy, entrapment
eosinophilia-myalgia M35.89
epileptic — see also Epilepsy, by type
absence G40.A09
intractable G40.A19
with status epilepticus G40.A11
without status epilepticus G40.A19
not intractable G40.A09
with status epilepticus G40.A01
without status epilepticus G40.A09
Erdheim-Chester (ECD) E88.89
Erdheim's E22.0
erythrocyte fragmentation D59.4
Evans D69.41
exhaustion F48.8
extrapyramidal G25.9
specified NEC G25.89
eye retraction — see Strabismus
eyelid-malar-mandible Q87.0
Faber's D50.9
facet M47.89-
facet joint M47.819 — see also Spondylosis
facial pain, paroxysmal G50.0
Fallot's Q21.3
familial cancer
with
pathogenic BRCA1 mutation QA1.790
pathogenic BRCA2 mutation QA1.791
familial cold autoinflammatory M04.2
familial eczema-thrombocytopenia (Wiskott-Aldrich) D82.0
Fanconi (-de Toni) (-Debré) E72.09
with cystinosis E72.04
fatigue
chronic G93.32
postviral G93.31
psychogenic F48.8
faulty bowel habit K59.39
Feil-Klippel (brevicollis) Q76.1
Felty's — see Felty's syndrome
fertile eunuch E23.0
fetal
alcohol (dysmorphic) Q86.0
hydantoin Q86.1
Fiedler's I40.1
first arch Q87.0
fish odor E72.89
Fisher's G61.0
Fitzhugh-Curtis
due to
Chlamydia trachomatis A74.81
Neisseria gonorrhea (gonococcal peritonitis) A54.85
Fitz's K85.80 — see also Pancreatitis, acute
Flajani (-Basedow) E05.00
with thyroid storm E05.01
flatback — see Flatback syndrome
floppy
baby P94.2
iris (intraoeprative) (IFIS) H21.81
mitral valve I34.1
flush E34.09
Foix-Alajouanine G95.19
Fong's Q87.2
food protein-induced enterocolitis (FPIES) K52.21
foramen magnum G93.5
Foster-Kennedy H47.14-
Foville's (peduncular) G46.3
FOXG1 QA0.0151
fragile X Q99.2
Franceschetti Q75.4
Frey's
auriculotemporal G50.8
hyperhidrosis L74.52
Friderichsen-Waterhouse A39.1
Froin's G95.89
frontal lobe F07.0
Fukuhara E88.49
functional
bowel K59.9
prepubertal castrate E29.1
Gaisböck's D75.1
ganglion (basal ganglia brain) G25.9
geniculi G51.1
Gardner-Diamond D69.2
gastroesophageal
junction K22.0
laceration-hemorrhage K22.6
gastrojejunal loop obstruction K91.89
Gee-Herter-Heubner K90.0
Gelineau's G47.419
with cataplexy G47.411
genito-anorectal A55
Gerstmann-Sträussler-Scheinker (GSS) A81.82
Gianotti-Crosti L44.4
giant platelet (Bernard-Soulier) D69.19
Gilles de la Tourette's F95.2
Glass Q87.89
Gleich's D72.118
goiter-deafness E07.1
Goldberg Q89.89
Goldberg-Maxwell E34.51
Good's D83.8
Gopalan's (burning feet) E53.8
Gorlin's Q87.89
Gougerot-Blum L81.7
Gouley's I31.1
Gower's R55
gray or grey (newborn) P93.0
platelet D69.19
Gubler-Millard G46.3
Guillain-Barré (-Strohl) G61.0
Gulf war T75.830
gustatory sweating G50.8
Hadfield-Clarke K86.89
hair tourniquet — see Constriction, external, by site
Hamman's J98.19
hand-foot L27.1
hand-shoulder G90.89
hantavirus (cardio)-pulmonary (HPS) (HCPS) B33.4
Hao-Fountain (HAFOUS) Q87.87
happy puppet Q93.51
Harada's H30.81-
Hayem-Faber D50.9
headache NEC G44.89
complicated NEC G44.59
Heberden's I20.89
Hedinger's E34.01
Hegglin's D72.0
HELLP (hemolysis, elevated liver enzymes and low platelet count) O14.2-
complicating
childbirth O14.24
puerperium O14.25
hemolytic-uremic D59.30
atypical D59.39
genetic D59.32
hereditary D59.32
infection-associated D59.31
secondary D59.39
specified NEC D59.39
due to genetic disorder D59.32
familial D59.32
hereditary D59.32
infection-associated D59.31
secondary D59.39
Shiga toxin-producing E. coli [STEC] related D59.31
specified NEC D59.39
typical D59.31
hemophagocytic, infection-associated D76.2
Henoch-Schönlein D69.0
hepatic flexure K59.89
hepatopulmonary K76.81
hepatorenal K76.7
following delivery O90.41
postoperative or postprocedural K91.83
postpartum, puerperal O90.41
hepatourologic K76.7
hereditary alpha tryptasemia D89.44
hereditary breast and ovarian cancer
with
pathogenic BRCA1 mutation QA1.790
pathogenic BRCA2 mutation QA1.791
Herter (-Gee) (nontropical sprue) K90.0
Heubner-Herter K90.0
Heyd's K76.7
Hilger's G90.09
histamine-like (fish poisoning) — see Poisoning, fish
histiocytic D76.3
histiocytosis NEC D76.3
HIV infection, acute B20
Hoffmann-Werdnig G12.0
Hollander-Simons E88.19
Hoppe-Goldflam G70.00
with exacerbation (acute) G70.01
in crisis G70.01
Horner's G90.2
hungry bone E83.81
hunterian glossitis D51.0
Hunt's (herpetic geniculate ganglionitis) (neuralgia) B02.21
dyssynergia cerebellaris myoclonica G11.19
Hutchinson's triad A50.53
hyperabduction G54.0
hyperammonemia-hyperornithinemia-homocitrullinemia E72.4
hypereosinophilic (HES) D72.119
idiopathic (IHES) D72.110
lymphocytic variant (LHES) D72.111
myeloid D72.118
specified NEC D72.118
hyperimmunoglobulin D M04.1
hyperimmunoglobulin E (IgE) D82.4
hyperkalemic E87.5
hyperkinetic — see Hyperkinesia
hypermobility M35.7
hypernatremia E87.0
hyperosmolarity (see also, Diabetes, by type, with hyperosmolarity) E87.0
hyperperfusion G97.82
hypersplenic D73.1
hypertransfusion, newborn P61.1
hyperventilation F45.8
hyperviscosity ( of serum)
polycythemic D75.1
sclerothymic D58.8
hypoglycemic (familial) (neonatal) E16.2
hypokalemic E87.6
hyponatremic E87.1
hypopituitarism E23.0
hypoplastic left-heart Q23.4
hypopotassemia E87.6
hyposmolality E87.1
hypotension, maternal O26.5-
hypothenar hammer I73.89
hypoventilation, obesity (OHS) E66.2
ICF (intravascular coagulation-fibrinolysis) D65
idiopathic
cardiorespiratory distress, newborn P22.0
nephrotic (infantile) N04.9
iliotibial band M76.3-
immobility, immobilization (paraplegic) M62.3
immune effector cell-associated neurotoxicity (ICANS) G92.00
grade
1 G92.01
2 G92.02
3 G92.03
4 G92.04
5 G92.05
unspecified G92.00
immune reconstitution D89.3
immune reconstitution inflammatory [IRIS] D89.3
immunity deficiency, combined D81.9
immunodeficiency
acquired — see Human, immunodeficiency virus (HIV) disease
combined D81.9
impending coronary I20.0
impingement, shoulder M75.4-
inappropriate secretion of antidiuretic hormone E22.2
infant
of diabetic mother P70.1
gestational diabetes P70.0
infantilism (pituitary) E23.0
inferior vena cava I87.1
inherited neoplasm predisposition syndrome of multiple systems, specified NEC QA1.798
inspissated bile (newborn) P59.1
institutional (childhood) F94.2
insufficient sleep F51.12
insulin resistance
type A E88.811
type B E88.818
intermediate coronary (artery) I20.0
interspinous ligament — see Spondylopathy, specified NEC
intestinal
carcinoid E34.09
knot K56.2
intravascular coagulation-fibrinolysis (ICF) D65
iodine-deficiency, congenital E00.9
type
mixed E00.2
myxedematous E00.1
neurological E00.0
IRDS (idiopathic respiratory distress, newborn) P22.0
irritable
bowel K58.9
with
constipation K58.1
diarrhea K58.0
mixed K58.2
psychogenic F45.8
specified NEC K58.8
heart (psychogenic) F45.8
weakness F48.8
ischemic
bowel (transient) K55.9
chronic K55.1
due to mesenteric artery insufficiency K55.1
steal T82.898
IVC (intravascular coagulopathy) D65
Ivemark's Q89.01
Jaccoud's — see Arthropathy, postrheumatic, chronic
Jackson's G83.89
Jakob-Creutzfeldt — see Creutzfeldt-Jakob disease or syndrome
jaw-winking Q07.8
Jervell-Lange-Nielsen I45.81
jet lag G47.25
Job's D71.8
Joseph-Diamond-Blackfan D61.01
jugular foramen G52.7
Kabuki (type 1, due to KMT2D mutation) (type 2, due to KDM6A mutation) Q89.81
Kanner's (autism) F84.0
Kartagener's Q89.3
Kelly's D50.1
Kimmelstiel-Wilson — see Diabetes, specified type, with Kimmelstiel-Wilson disease
Kleefstra Q87.86
Klein (e)-Levine G47.13
Klippel-Feil (brevicollis) Q76.1
Köhler-Pellegrini-Stieda — see Bursitis, tibial collateral
König's K59.89
Korsakoff (-Wernicke) (nonalcoholic) F04
alcoholic F10.9-
with dependence F10.2-
Kostmann's D70.0
Krabbe's congenital muscle hypoplasia Q79.8
labyrinthine
lacunar NEC G46.7
Lambert-Eaton G70.80
in
neoplastic disease G73.1
specified disease NEC G70.81
Landau-Kleffner — see Epilepsy, specified NEC
Larsen's Q74.8
Lassueur Graham-Little Piccardi L66.19
lateral
cutaneous nerve of thigh G57.1-
medullary G46.4
Launois' E22.0
Laurence-Moon Q87.84
Lawrence E88.12
lazy
leukocyte D70.8
posture M62.3
Lemierre I80.8
Lennox-Gastaut G40.812
intractable G40.814
with status epilepticus G40.813
without status epilepticus G40.814
not intractable G40.812
with status epilepticus G40.811
without status epilepticus G40.812
lenticular, progressive E83.01
Leopold-Levi's E05.90
Lev's I44.2
Li-Fraumeni QA1.792
Lichtheim's D51.0
Lightwood's N25.89
Lignac (de Toni) (-Fanconi) (-Debré) E72.09
with cystinosis E72.04
Likoff's I20.89
limbic epilepsy personality F07.0
liver-kidney K76.7
lobotomy F07.0
Loeys-Dietz Q87.A
Löffler's J82.89
long arm 18 or 21 deletion Q93.89
long QT I45.81
Louis-Barré G11.3
low
atmospheric pressure T70.29
back M54.50
output (cardiac) I50.9
lower radicular, newborn (birth injury) P14.8
Luetscher's (dehydration) E86.0
Lupus anticoagulant D68.62
Lutembacher's Q21.19
Lynch (due to EPCAM) (due to MLH1) (due to MSH2) (due to MSH6) (due to PMS2) QA1.71
macrophage activation D76.1
due to infection D76.2
magnesium-deficiency R29.0
Majeed M04.8
Mal de Debarquement R42
malabsorption K90.9
postsurgical K91.2
malformation, congenital, due to
alcohol Q86.0
exogenous cause NEC Q86.8
hydantoin Q86.1
warfarin Q86.2
malignant
carcinoid E34.00
neuroleptic G21.0
Mallory-Weiss K22.6
mandibulofacial dysostosis Q75.4
manic-depressive — see Disorder, bipolar
maple-syrup-urine E71.0
Marable's I77.4
Marfan Q87.40
with
cardiovascular manifestations Q87.418
aortic dilation Q87.410
ocular manifestations Q87.42
skeletal manifestations Q87.43
Marie's (acromegaly) E22.0
mast cell activation — see Activation, mast cell
maternal hypotension — see Syndrome, hypotension, maternal
May (-Hegglin) D72.0
McArdle (-Schmidt) (-Pearson) E74.04
McQuarrie's E16.2
meconium plug (newborn) P76.0
MED13L (mediator complex subunit 13L) Q87.85
median arcuate ligament I77.4
mediator complex subunit 13L (MED13L) Q87.85
Meekeren-Ehlers-Danlos Q79.6
megavitamin-B6 E67.2
Meige G24.4
MELAS E88.41
Mendelson's O74.0
MERRF (myoclonic epilepsy associated with ragged-red fibers) E88.42
mesenteric
artery (superior) K55.1
vascular insufficiency K55.1
metabolic E88.810
metastatic carcinoid E34.00
micrognathia-glossoptosis Q87.0
midbrain NEC G93.89
middle lobe (lung) J98.19
middle radicular G54.0
migraine G43.909- — see also Migraine
Mikulicz' K11.8
milk-alkali E83.52
Millard-Gubler G46.3
Miller-Dieker Q93.88
Miller-Fisher G61.0
Minkowski-Chauffard D58.0
Mirizzi's K83.1
MNGIE (Mitochondrial Neurogastrointestinal Encephalopathy) E88.49
Möbius, ophthalmoplegic migraine — see Migraine, ophthalmoplegic
monofixation H50.42
Morel-Moore M85.2
Morel-Morgagni M85.2
Morgagni (-Morel) (-Stewart) M85.2
Morgagni-Adams-Stokes I45.9
Muckle-Wells M04.2
mucocutaneous lymph node (acute febrile) (MCLS) M30.3
multiple endocrine neoplasia (MEN) — see Neoplasia, endocrine, multiple (MEN)
multiple operations — see Disorder, factitious
multisystem inflammatory (in adults) (in children) M35.81
Mounier-Kuhn Q32.4
with bronchiectasis J47.9
with
exacerbation (acute) J47.1
lower respiratory infection J47.0
acquired J98.09
with bronchiectasis J47.9
with
exacerbation (acute) J47.1
lower respiratory infection J47.0
myasthenic G70.9
in
diabetes mellitus — see Diabetes, amyotrophy
endocrine disease NEC E34.9
neoplastic disease D49.9 — see also Neoplasm
thyrotoxicosis (hyperthyroidism) E05.90
with thyroid storm E05.91
myelodysplastic D46.9
with
5q deletion D46.C
isolated del (5q) chromosomal abnormality D46.C
multilineage dysplasia D46.A
with ringed sideroblasts D46.B
pancytopenia (acquired) D61.818
lesions, low grade D46.20
specified NEC D46.Z
myeloid hypereosinophilic D72.118
myelopathic pain G89.0
myeloproliferative (chronic) D47.1
myofascial pain M79.18
Naffziger's G54.0
nail patella Q87.2
NARP (Neuropathy, Ataxia and Retinitis pigmentosa) E88.49
neonatal abstinence P96.1
nephritic — see also Nephritis
with edema — see Nephrosis
acute N00.9
chronic N03.9
rapidly progressive N01.9
nephrotic (congenital) N04.9 — see also Nephrosis
with
C3
glomerulonephritis N04.A
glomerulopathy N04.A
with dense deposit disease N04.6
dense deposit disease N04.6
diffuse
crescentic glomerulonephritis N04.7
endocapillary proliferative glomerulonephritis N04.4
membranous glomerulonephritis N04.20
mesangial proliferative glomerulonephritis N04.3
mesangiocapillary glomerulonephritis N04.5
focal and segmental glomerular lesions N04.1
minor glomerular abnormality N04.0
specified morphological changes NEC N04.8
diabetic — see Diabetes, nephrosis
specified type NEC with diffuse membranous glomerulonephritis N04.29
neurologic neglect R41.4
Nezelof's D81.4
Niikawa-Kuroki Q89.81
Nonne-Milroy-Meige Q82.0
Nothnagel's vasomotor acroparesthesia I73.89
obesity hypoventilation (OHS) E66.2
obliterans
bronchiolitis J44.81 — see also Bronchiolitis, obliterative
oculomotor H51.9
Ogilvie K59.81
Oliver-McFarlane Q87.89
ophthalmoplegia-cerebellar ataxia — see Strabismus, paralytic, third nerve
oral allergy T78.19
oral-facial-digital Q87.0
organic
affective F06.30
amnesic (not alcohol- or drug-induced) F04
brain F09
depressive F06.31
hallucinosis F06.0
personality F07.0
Ormond's N13.5
oro-facial-digital Q87.0
os trigonum Q68.8
Osler-Weber-Rendu I78.0
osteoporosis-osteomalacia M83.8
Osterreicher-Turner Q87.2
otolith
oto-palatal-digital Q87.0
outlet (thoracic) G54.0 — see also Syndrome, thoracic outlet
ovary
polycystic E28.2
resistant E28.39
sclerocystic E28.2
Owren's D68.2
Paget-Schroetter I82.890
pain — see also Pain
complex regional I G90.50
lower limb G90.52-
specified site NEC G90.59
upper limb G90.51-
complex regional II — see Causalgia
painful
bruising D69.2
feet E53.8
prostate N42.81
paralysis agitans — see Parkinsonism
paralytic G83.9
specified NEC G83.89
Parinaud's H51.0
parkinsonian — see Parkinsonism
Parkinson's — see Parkinsonism
paroxysmal facial pain G50.0
Parry's E05.00
with thyroid storm E05.01
Parsonage (-Aldren)-Turner G54.5
patella clunk M25.86-
Paterson (-Brown) (-Kelly) D50.1
pectoral girdle I77.89
pectoralis minor I77.89
pediatric acute-onset neuropsychiatric (PANS) D89.89
pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections (PANDAS) D89.89
pediatric inflammatory multisystem M35.81
Pelger-Huet D72.0
pellagra-cerebellar ataxia-renal aminoaciduria E72.02
pellagroid E52
Pellegrini-Stieda — see Bursitis, tibial collateral
pelvic congestion-fibrosis, female N94.89
penta X Q97.1
peptic ulcer — see Ulcer, peptic
perabduction I77.89
periodic fever M04.1
periodic fever, aphthous stomatitis, pharyngitis, and adenopathy [PFAPA] M04.8
periodic headache, in adults and children — see Headache, periodic syndromes in adults and children
periurethral fibrosis N13.5
Peutz-Jeghers Q85.89
phantom limb (without pain) G54.7
with pain G54.6
pharyngeal pouch D82.1
Phelan-McDermid Q93.52
Pick's — see Disease, Pick's
Pickwickian E66.2
PIE (pulmonary infiltration with eosinophilia) J82.89 — see also Eosinophilia, pulmonary
pigmentary pallidal degeneration (progressive) G23.0
pineal E34.8
pituitary E22.0
plantar fascia M72.2-
placental transfusion — see Pregnancy, complicated by, placental transfusion syndromes
plateau iris (post-iridectomy) (postprocedural) H21.82
Plummer-Vinson D50.1
pluricarential of infancy E40
plurideficiency E40
pluriglandular (compensatory) E31.8
autoimmune E31.0
pneumatic hammer T75.21
polyangiitis overlap M30.8
polycarential of infancy E40
polyglandular E31.8
autoimmune E31.0
polysplenia Q89.09
pontine NEC G93.89
popliteal
artery entrapment I77.89
web Q87.89
postbacterial fatigue G93.39
postcardiac injury
postcardiotomy I97.0
postmyocardial infarction I24.1
postcardiotomy I97.0
post chemoembolization - code to associated conditions
postcholecystectomy K91.5
postcommissurotomy I97.0
postconcussional F07.81
postcontusional F07.81
post-COVID (-19) U09.9
postencephalitic F07.89
post endometrial ablation N99.85
post-polypectomy coagulation K91.89
posterior
cervical sympathetic M53.0
cord G83.83
fossa compression G93.5
reversible encephalopathy (PRES) I67.83
postgastrectomy (dumping) K91.1
postgastric surgery K91.1
postinfarction I24.1
postinfectious fatigue G93.39
postlaminectomy NEC M96.1
postleukotomy F07.0
postmastectomy lymphedema I97.2
postmyocardial infarction I24.1
postoperative NEC T81.9
blind loop K90.2
postpartum panhypopituitary (Sheehan) E23.0
postpolio (myelitic) G14
postthrombotic I87.009
with
inflammation I87.02-
with ulcer I87.03-
specified complication NEC I87.09-
ulcer I87.01-
with inflammation I87.03-
asymptomatic I87.00-
postural
orthostatic tachycardia [POTS] G90.A
tachycardia G90.A
postvagotomy K91.1
postvalvulotomy I97.0
postviral NEC G93.31
fatigue G93.31
Potain's K31.0
potassium intoxication E87.5
Prader-Willi Q87.11
Prader-Willi-like Q87.19
precerebral artery (multiple) (bilateral) G45.2
preinfarction I20.0
preleukemic D46.9
premature senility E34.8
premenstrual dysphoric F32.81
premenstrual tension N94.3
Prinzmetal-Massumi R07.1
prune belly Q79.4
pseudocarpal tunnel (sublimis) — see Syndrome, carpal tunnel
pseudoparalytica G70.00
with exacerbation (acute) G70.01
in crisis G70.01
pseudo -Turner's Q87.19
psycho-organic (nonpsychotic severity) F07.9
acute or subacute F05
depressive type F06.31
hallucinatory type F06.0
nonpsychotic severity F07.0
specified NEC F07.89
PTEN (hamartoma) tumor Q85.81
pulmonary
arteriosclerosis I27.0
dysmaturity (Wilson-Mikity) P27.0
hypoperfusion (idiopathic) P22.0
renal (hemorrhagic) (Goodpasture's) M31.0
pure
motor lacunar G46.5
sensory lacunar G46.6
Putnam-Dana D51.0
pyogenic arthritis, pyoderma gangrenosum, and acne [PAPA] M04.8
pyramidopallidonigral G20.C
pyriformis — see Lesion, nerve, sciatic
QT interval prolongation I45.81
radicular NEC — see Radiculopathy
upper limbs, newborn (birth injury) P14.3
rapid time-zone change G47.25
Rasmussen G04.81
Raymond (-Céstan) I65.8
Raynaud's I73.00
with gangrene I73.01
RDS (respiratory distress syndrome, newborn) P22.0
reactive airways dysfunction J68.3
Refsum's G60.1
Reifenstein E34.52
renal glomerulohyalinosis-diabetic — see Diabetes, nephrosis
Rendu-Osler-Weber I78.0
residual ovary N99.83
resistant ovary E28.39
respiratory
distress
acute J80
adult J80
child J80
idiopathic J84.114
newborn (idiopathic) (type I) P22.0
type II P22.1
restless legs G25.81
restrictive allograft J4A.0
retinoblastoma (familial) C69.2
retroperitoneal fibrosis K68.2
retroviral seroconversion (acute) Z21
Reye's G93.7
Richter — see Leukemia, chronic lymphocytic, B-cell type
Ridley's I50.1
right
heart, hypoplastic Q22.6
ventricular obstruction — see Failure, heart, right
Romano-Ward (prolonged QT interval) I45.81
rotator cuff, shoulder M75.10- — see also Tear, rotator cuff
Rotes Quérol — see Hyperostosis, ankylosing
Roth — see Meralgia paresthetica
rubella (congenital) P35.0
Ruvalcaba-Myhre-Smith E71.440
Rytand-Lipsitch I44.2
salt
depletion E87.1
due to heat NEC T67.8
causing heat exhaustion or prostration T67.4
low E87.1
salt-losing N28.89
SATB2-associated Q87.89
Scaglietti-Dagnini E22.0
scalenus anticus (anterior) G54.0
scapulocostal — see Mononeuropathy, upper limb, specified site NEC
scapuloperoneal G71.09
schizophrenic, of childhood NEC F20.9
Schnitzler D47.2
Scholte's E34.09
Schroeder's E27.0
Schüller-Christian C96.5
Schwachman (-Diamond) D61.02
Schwartz (-Jampel) G71.13
Schwartz-Bartter E22.2
scimitar Q26.8
sclerocystic ovary E28.2
Seitelberger's G31.89
septicemic adrenal hemorrhage A39.1
seroconversion, retroviral (acute) Z21
serotonin G90.81
serous meningitis G93.2
severe acute respiratory (SARS) J12.81
coronavirus 2 U07.1 — see also COVID-19
pneumonia J12.82
shaken infant T74.4
shock (traumatic) T79.4
kidney N17.0
following crush injury T79.5
toxic A48.3
shock-lung J80
Shone's - code to specific anomalies
short
bowel K90.829
with
colon in continuity K90.821
ileocolonic anastomosis K90.821
without colon in continuity K90.822
gut — see Syndrome, short, bowel
rib Q77.2
shoulder-hand — see Algoneurodystrophy
Shwachman (-Diamond) D61.02
sicca — see Syndrome, Sjögren
sick
cell E87.1
sinus I49.5
sick-euthyroid E07.81
sideropenic D50.1
Siemens' ectodermal dysplasia Q82.4
Silfversköld's Q78.9
Simons' E88.11
sinus tarsi M25.57-
sinusitis-bronchiectasis-situs inversus Q89.3
Sipple's E31.22
sirenomelia Q87.2
Sjögren M35.00
with
central nervous system involvement M35.07
dental involvement M35.0C
gastrointestinal involvement M35.08
glomerular disease M35.0A
inflammatory arthritis M35.05
keratoconjunctivitis M35.01
lung involvement M35.02
myopathy M35.03
peripheral nervous system involvement M35.06
renal tubular acidosis M35.04
specified organ involvement, NEC M35.09
tubulo-interstitial nephropathy M35.04
vasculitis M35.0B
Slocumb's E27.0
slow flow, coronary I20.89
Sluder's G44.89
Smith-Magenis Q93.88
Sneddon-Wilkinson L13.1
Snyder-Robinson Q87.89
Soto's Q87.3
South African cardiomyopathy I42.89
spasmodic
upward movement, eyes H51.8
winking F95.8
Spen's I45.9
splenic
agenesis Q89.01
flexure K59.89
neutropenia D73.81
Spurway's Q78.0
staphylococcal scalded skin L00
steal
arteriovenous T82.898-
ischemic T82.898-
subclavian G45.8
Stein-Leventhal E28.2
Stein's E28.2
Stevens-Johnson syndrome L51.1
toxic epidermal necrolysis overlap L51.3
Stewart-Morel M85.2
Stickler Q89.89
stiff baby Q89.89
stiff man G25.82
Still-Felty — see Felty's syndrome
Stokes (-Adams) I45.9
stone heart I50.1
straight back, congenital Q76.49
Sturge-Weber (-Dimitri) Q85.89
subclavian steal G45.8
subcoracoid-pectoralis minor G54.0
subcostal nerve compression I77.89
subphrenic interposition Q43.3
superior
cerebellar artery I63.89
mesenteric artery K55.1
semi-circular canal dehiscence H83.8X-
vena cava I87.1
supine hypotensive (maternal) — see Syndrome, hypotension, maternal
suprarenal cortical E27.0
supraspinatus M75.10- — see also Tear, rotator cuff
Susac G93.49
swallowed blood P78.2
sweat retention L74.0
Swyer Q99.1
Symond's G93.2
sympathetic
cervical paralysis G90.2
pelvic, female N94.89
systemic inflammatory response (SIRS), of non-infectious origin (without organ dysfunction) R65.10
with acute organ dysfunction R65.11
tachycardia-bradycardia I49.5
takotsubo I51.81
TAR (thrombocytopenia with absent radius) Q87.2
tarsal tunnel G57.5-
teething K00.7
tegmental G93.89
telangiectasic-pigmentation-cataract Q82.8
temporal pyramidal apex — see Otitis, media, suppurative, acute
temporomandibular joint-pain-dysfunction M26.62-
Terry's H44.2- — see also Myopia, degenerative
testicular feminization E34.51 — see also Syndrome, androgen insensitivity
thalamic pain (hyperesthetic) G89.0
thoracic outlet (compression) G54.0
arterial I77.89
neurogenic G54.0
venous I87.1
Thorson-Björck E34.09
thrombocytopenia with absent radius (TAR) Q87.2
thrombosis with thrombocytopenia D75.84
thyroid-adrenocortical insufficiency E31.0
tibial
anterior M76.81-
posterior M76.82-
Tietze's M94.0
time-zone (rapid) G47.25
Toni-Fanconi E72.09
with cystinosis E72.04
Touraine's Q79.8
tourniquet — see Constriction, external, by site
toxic shock A48.3
transient left ventricular apical ballooning I51.81
traumatic vasospastic T75.22
Treacher Collins Q75.4
triple X, female Q97.0
trisomy Q92.9
13 Q91.7
meiotic nondisjunction Q91.4
mitotic nondisjunction Q91.5
mosaicism Q91.5
translocation Q91.6
18 Q91.3
meiotic nondisjunction Q91.0
mitotic nondisjunction Q91.1
mosaicism Q91.1
translocation Q91.2
20 (q)(p) Q92.8
21 Q90.9
meiotic nondisjunction Q90.0
mitotic nondisjunction Q90.1
mosaicism Q90.1
translocation Q90.2
22 Q92.8
tropical wet feet T69.02-
Trousseau's I82.1
tumor lysis (following antineoplastic chemotherapy) (spontaneous) NEC E88.3
tumor necrosis factor receptor associated periodic (TRAPS) M04.1
Twiddler's (due to)
automatic implantable defibrillator T82.198
cardiac pacemaker T82.198
Unverricht (-Lundborg) — see Epilepsy, generalized, idiopathic
upward gaze H51.8
uremia, chronic N18.9 — see also Disease, kidney, chronic
urethral N34.3
urethro-oculo-articular — see Reiter's disease
urohepatic K76.7
usher Q99.819
specified NEC Q99.818
type 1 Q99.811
type 2 Q99.812
type 3 Q99.813
type 4 Q99.818
vacuoles, E1 ubiquitin-activating enzyme, X-linked, autoinflammatory, somatic (VEXAS) M04.3
vago-hypoglossal G52.7
vanishing twin of one fetus or more O31.4-
vascular NEC in cerebrovascular disease G46.8
vasoconstriction, reversible cerebrovascular I67.841
vasomotor I73.9
vasospastic (traumatic) T75.22
vasovagal R55
van Buchem's M85.2
van der Hoeve's Q78.0
VATER Q87.2
velo-cardio-facial Q93.81
vena cava (inferior) (superior) (obstruction) I87.1
vertebral
artery G45.0
compression — see Syndrome, anterior, spinal artery, compression
steal G45.0
vertebro-basilar artery G45.0
vertebrogenic (pain) M54.89 — see also Pain, vertebrogenic
vertiginous — see Disorder, vestibular function
VEXAS (vacuoles, E1 ubiquitin-activating enzyme, X-linked, autoinflammatory, somatic) M04.3
Vinson-Plummer D50.1
virus B34.9
visceral larva migrans B83.0
visual disorientation H53.8
vitamin B6 deficiency E53.1
vitreal corneal H59.01-
vitreous (touch) H59.01-
Vogt-Koyanagi H20.82-
Volkmann's T79.6
von Hippel-Lindau Q85.83
von Schroetter's I82.890
von Willebrand (-Jürgen) — see Disease, von Willebrand
acquired D68.04 — see also Disease, von Willebrand
Waldenström-Kjellberg D50.1
Wallenberg's G46.3
wasting (syndrome) due to underlying condition E88.A
water retention E87.79
Waterhouse (-Friderichsen) A39.1
Weber-Gubler G46.3
Weber-Leyden G46.3
Weber's G46.3
Wegener's M31.30
with
kidney involvement M31.31
lung involvement M31.30
with kidney involvement M31.31
Weingarten's (tropical eosinophilia) J82.89
Weiss-Baker G90.09
Werdnig-Hoffman G12.0
Wermer's E31.21
Werner's E34.8
Wernicke-Korsakoff (nonalcoholic) F04
alcoholic F10.9-
with dependence F10.2-
West's — see Epilepsy, spasms
Westphal-Strümpell E83.01
wet
feet (maceration) (tropical) T69.02-
lung, newborn P22.1
whiplash S13.4
whistling face Q87.0
Wilkie's K55.1
Wilkinson-Sneddon L13.1
Williams Q93.82
Willebrand (-Jürgens) — see Disease, von Willebrand
Wilson's (hepatolenticular degeneration) E83.01
Wiskott-Aldrich D82.0
withdrawal — see Withdrawal, state
drug
infant of dependent mother P96.1
therapeutic use, newborn P96.2
Woakes' (ethmoiditis) J33.1
Wright's (hyperabduction) G54.0
X I20.9
XXXX Q97.1
XXXXX Q97.1
XXXXY Q98.1
XXY Q98.0
Yao M04.8
yellow nail L60.5
Zahorsky's B08.5
Zellweger syndrome E71.510
Zellweger-like syndrome E71.541