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Syndrome

Disease index · Modifiers and references

Modifiers and references · icd10cm-index-2027.xml

Syndrome › Ehlers-Danlos

classical(cEDS) (classical EDS)

Q79.61

Syndrome › Ehlers-Danlos

hypermobile(hEDS) (hypermobile EDS)

Q79.62

Syndrome › Ehlers-Danlos

specified NEC

Q79.69

Syndrome › Ehlers-Danlos

vascular(vascular EDS) (vEDS)

Q79.63

Syndrome

electric feet

E53.8

Syndrome

Ellis-van Creveld

Q77.6

Syndrome

endocrine-hypertensive

E27.0

Syndrome

entrapment

See: Neuropathy, entrapment

Syndrome

eosinophilia-myalgia

M35.89

Syndrome

epileptic

See also: Epilepsy, by type

Syndrome › epileptic

absence

G40.A09

Syndrome › epileptic › absence

intractable

G40.A19

Syndrome › epileptic › absence › intractable

with status epilepticus

G40.A11

Syndrome › epileptic › absence › intractable

without status epilepticus

G40.A19

Syndrome › epileptic › absence

not intractable

G40.A09

Syndrome › epileptic › absence › not intractable

with status epilepticus

G40.A01

Syndrome › epileptic › absence › not intractable

without status epilepticus

G40.A09

Syndrome

Erdheim-Chester(ECD)

E88.89

Syndrome

erythrocyte fragmentation

D59.4

Syndrome

extrapyramidal

G25.9

Syndrome › extrapyramidal

specified NEC

G25.89

Syndrome

eye retraction

See: Strabismus

Syndrome

eyelid-malar-mandible

Q87.0

Syndrome

facet joint

M47.819

See also: Spondylosis

Syndrome

facial pain, paroxysmal

G50.0

Syndrome

familial cancer

Syndrome › familial cancer

with

Syndrome › familial cancer › with

pathogenic BRCA1 mutation

QA1.790

Syndrome › familial cancer › with

pathogenic BRCA2 mutation

QA1.791

Syndrome

familial cold autoinflammatory

M04.2

Syndrome

familial eczema-thrombocytopenia(Wiskott-Aldrich)

D82.0

Syndrome

Fanconi(-de Toni) (-Debré)

E72.09

Syndrome › Fanconi(-de Toni) (-Debré)

with cystinosis

E72.04

Syndrome

fatigue

Syndrome › fatigue

chronic

G93.32

Syndrome › fatigue

postviral

G93.31

Syndrome › fatigue

psychogenic

F48.8

Syndrome

faulty bowel habit

K59.39

Syndrome

Feil-Klippel(brevicollis)

Q76.1

Syndrome

Felty's

See: Felty's syndrome

Syndrome

fertile eunuch

E23.0

Syndrome

fetal

Syndrome › fetal

alcohol(dysmorphic)

Q86.0

Syndrome › fetal

hydantoin

Q86.1

Syndrome

Fitzhugh-Curtis

Syndrome › Fitzhugh-Curtis

due to

Syndrome › Fitzhugh-Curtis › due to

Chlamydia trachomatis

A74.81

Syndrome › Fitzhugh-Curtis › due to

Neisseria gonorrhea(gonococcal peritonitis)

A54.85

Syndrome

Fitz's

K85.80

See also: Pancreatitis, acute

Syndrome

Flajani(-Basedow)

E05.00

Syndrome › Flajani(-Basedow)

with thyroid storm

E05.01

Syndrome

flatback

See: Flatback syndrome

Syndrome

floppy

Syndrome › floppy

baby

P94.2

Syndrome › floppy

iris(intraoeprative) (IFIS)

H21.81

Syndrome › floppy

mitral valve

I34.1

Syndrome

Foix-Alajouanine

G95.19

Syndrome

food protein-induced enterocolitis(FPIES)

K52.21

Syndrome

foramen magnum

G93.5

Syndrome

Foville's(peduncular)

G46.3

Syndrome

Franceschetti

Q75.4

Syndrome

Frey's

Syndrome › Frey's

auriculotemporal

G50.8

Syndrome › Frey's

hyperhidrosis

L74.52

Syndrome

Friderichsen-Waterhouse

A39.1

Syndrome

frontal lobe

F07.0

Syndrome

functional

Syndrome › functional

bowel

K59.9

Syndrome › functional

prepubertal castrate

E29.1

Syndrome

ganglion(basal ganglia brain)

G25.9

Syndrome › ganglion(basal ganglia brain)

geniculi

G51.1

Syndrome

Gardner-Diamond

D69.2

Syndrome

gastroesophageal

Syndrome › gastroesophageal

junction

K22.0

Syndrome › gastroesophageal

laceration-hemorrhage

K22.6

Syndrome

gastrojejunal loop obstruction

K91.89

Syndrome

Gee-Herter-Heubner

K90.0

Syndrome › Gelineau's

with cataplexy

G47.411

Syndrome

genito-anorectal

A55

Syndrome

Gerstmann-Sträussler-Scheinker(GSS)

A81.82

Syndrome

Gianotti-Crosti

L44.4

Syndrome

giant platelet(Bernard-Soulier)

D69.19

Syndrome

Gilles de la Tourette's

F95.2

Syndrome

goiter-deafness

E07.1

Syndrome

Goldberg-Maxwell

E34.51

Syndrome

Gopalan's(burning feet)

E53.8

Syndrome

Gougerot-Blum

L81.7

Syndrome

Gower's

R55

Syndrome

gray or grey(newborn)

P93.0

Syndrome › gray or grey(newborn)

platelet

D69.19

Syndrome

Gubler-Millard

G46.3

Syndrome

Guillain-Barré(-Strohl)

G61.0

Syndrome

gustatory sweating

G50.8

Syndrome

hair tourniquet

See: Constriction, external, by site

Syndrome

hantavirus(cardio)-pulmonary (HPS) (HCPS)

B33.4

Syndrome

Hao-Fountain(HAFOUS)

Q87.87

Syndrome › headache NEC

complicated NEC

G44.59

Syndrome

HELLP(hemolysis, elevated liver enzymes and low platelet count)

O14.2-

Syndrome › HELLP(hemolysis, elevated liver enzymes and low platelet count)

complicating

Syndrome › HELLP(hemolysis, elevated liver enzymes and low platelet count) › complicating

childbirth

O14.24

Syndrome › HELLP(hemolysis, elevated liver enzymes and low platelet count) › complicating

puerperium

O14.25

Syndrome

hemolytic-uremic

D59.30

Syndrome › hemolytic-uremic

atypical

D59.39

Syndrome › hemolytic-uremic › atypical

genetic

D59.32

Syndrome › hemolytic-uremic › atypical

hereditary

D59.32

Syndrome › hemolytic-uremic › atypical

infection-associated

D59.31

Syndrome › hemolytic-uremic › atypical

secondary

D59.39

Syndrome › hemolytic-uremic › atypical

specified NEC

D59.39

Syndrome › hemolytic-uremic

due to genetic disorder

D59.32

Syndrome › hemolytic-uremic

familial

D59.32

Syndrome › hemolytic-uremic

hereditary

D59.32

Syndrome › hemolytic-uremic

infection-associated

D59.31

Syndrome › hemolytic-uremic

secondary

D59.39

Syndrome › hemolytic-uremic

Shiga toxin-producing E. coli [STEC] related

D59.31

Syndrome › hemolytic-uremic

specified NEC

D59.39

Syndrome › hemolytic-uremic

typical

D59.31

Syndrome

hemophagocytic, infection-associated

D76.2

Syndrome

Henoch-Schönlein

D69.0

Syndrome › hepatorenal

following delivery

O90.41

Syndrome › hepatorenal

postoperative or postprocedural

K91.83

Syndrome › hepatorenal

postpartum, puerperal

O90.41

Syndrome

hepatourologic

K76.7

Syndrome

hereditary alpha tryptasemia

D89.44

Syndrome

hereditary breast and ovarian cancer

Syndrome › hereditary breast and ovarian cancer

with

Syndrome › hereditary breast and ovarian cancer › with

pathogenic BRCA1 mutation

QA1.790

Syndrome › hereditary breast and ovarian cancer › with

pathogenic BRCA2 mutation

QA1.791

Syndrome

Herter(-Gee) (nontropical sprue)

K90.0

Syndrome

Heubner-Herter

K90.0

Syndrome

histamine-like(fish poisoning)

See: Poisoning, fish

Syndrome

histiocytosis NEC

D76.3

Syndrome

HIV infection, acute

B20

Syndrome

Hoffmann-Werdnig

G12.0

Syndrome

Hollander-Simons

E88.19

Syndrome › Hoppe-Goldflam

with exacerbation(acute)

G70.01

Syndrome › Hoppe-Goldflam

in crisis

G70.01

Syndrome

hunterian glossitis

D51.0

Syndrome

Hunt's(herpetic geniculate ganglionitis) (neuralgia)

B02.21

Syndrome › Hunt's(herpetic geniculate ganglionitis) (neuralgia)

dyssynergia cerebellaris myoclonica

G11.19

Syndrome

Hutchinson's triad

A50.53

Syndrome

hyperabduction

G54.0

Syndrome

hyperammonemia-hyperornithinemia-homocitrullinemia

E72.4

Syndrome

hypereosinophilic(HES)

D72.119

Syndrome › hypereosinophilic(HES)

idiopathic(IHES)

D72.110

Syndrome › hypereosinophilic(HES)

lymphocytic variant(LHES)

D72.111

Syndrome › hypereosinophilic(HES)

myeloid

D72.118

Syndrome › hypereosinophilic(HES)

specified NEC

D72.118

Syndrome

hyperimmunoglobulin D

M04.1

Syndrome

hyperimmunoglobulin E(IgE)

D82.4

Syndrome

hyperkalemic

E87.5