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Krankheitsverzeichnis

Syndrome

Krankheitsverzeichnis · Modifikatoren und Verweise

Modifikatoren und Verweise · icd10cm-index-April-1-2026-XML.xml

Syndrome

hypoglycemic(familial) (neonatal)

E16.2

Syndrome

hyponatremic

E87.1

Syndrome

hypopituitarism

E23.0

Syndrome

hypoplastic left-heart

Q23.4

Syndrome

hypopotassemia

E87.6

Syndrome

hyposmolality

E87.1

Syndrome

hypotension, maternal

O26.5-

Syndrome

hypothenar hammer

I73.89

Syndrome

hypoventilation, obesity(OHS)

E66.2

Syndrome

ICF(intravascular coagulation-fibrinolysis)

D65

Syndrome

idiopathic

Syndrome › idiopathic

cardiorespiratory distress, newborn

P22.0

Syndrome › idiopathic

nephrotic(infantile)

N04.9

Syndrome

iliotibial band

M76.3-

Syndrome

immobility, immobilization(paraplegic)

M62.3

Syndrome

immune effector cell-associated neurotoxicity(ICANS)

G92.00

Syndrome › immune effector cell-associated neurotoxicity(ICANS)

grade

Syndrome › immune effector cell-associated neurotoxicity(ICANS) › grade

1

G92.01

Syndrome › immune effector cell-associated neurotoxicity(ICANS) › grade

2

G92.02

Syndrome › immune effector cell-associated neurotoxicity(ICANS) › grade

3

G92.03

Syndrome › immune effector cell-associated neurotoxicity(ICANS) › grade

4

G92.04

Syndrome › immune effector cell-associated neurotoxicity(ICANS) › grade

5

G92.05

Syndrome › immune effector cell-associated neurotoxicity(ICANS) › grade

unspecified

G92.00

Syndrome

immune reconstitution

D89.3

Syndrome

immune reconstitution inflammatory [IRIS]

D89.3

Syndrome

immunity deficiency, combined

D81.9

Syndrome

immunodeficiency

Syndrome › immunodeficiency

acquired

See: Human, immunodeficiency virus (HIV) disease

Syndrome › immunodeficiency

combined

D81.9

Syndrome

impending coronary

I20.0

Syndrome

impingement, shoulder

M75.4-

Syndrome

inappropriate secretion of antidiuretic hormone

E22.2

Syndrome

infant

Syndrome › infant

of diabetic mother

P70.1

Syndrome › infant

gestational diabetes

P70.0

Syndrome

infantilism(pituitary)

E23.0

Syndrome

inferior vena cava

I87.1

Syndrome

inspissated bile(newborn)

P59.1

Syndrome

institutional(childhood)

F94.2

Syndrome

insufficient sleep

F51.12

Syndrome

insulin resistance

Syndrome › insulin resistance

type A

E88.811

Syndrome › insulin resistance

type B

E88.818

Syndrome

intermediate coronary(artery)

I20.0

Syndrome

interspinous ligament

See: Spondylopathy, specified NEC

Syndrome

intestinal

Syndrome › intestinal

carcinoid

E34.09

Syndrome › intestinal

knot

K56.2

Syndrome

intravascular coagulation-fibrinolysis(ICF)

D65

Syndrome

iodine-deficiency, congenital

E00.9

Syndrome › iodine-deficiency, congenital

type

Syndrome › iodine-deficiency, congenital › type

mixed

E00.2

Syndrome › iodine-deficiency, congenital › type

myxedematous

E00.1

Syndrome › iodine-deficiency, congenital › type

neurological

E00.0

Syndrome

IRDS(idiopathic respiratory distress, newborn)

P22.0

Syndrome

irritable

Syndrome › irritable

bowel

K58.9

Syndrome › irritable › bowel

with

Syndrome › irritable › bowel › with

constipation

K58.1

Syndrome › irritable › bowel › with

diarrhea

K58.0

Syndrome › irritable › bowel

mixed

K58.2

Syndrome › irritable › bowel

psychogenic

F45.8

Syndrome › irritable › bowel

specified NEC

K58.8

Syndrome › irritable

heart(psychogenic)

F45.8

Syndrome › irritable

weakness

F48.8

Syndrome

ischemic

Syndrome › ischemic

bowel(transient)

K55.9

Syndrome › ischemic › bowel(transient)

chronic

K55.1

Syndrome › ischemic › bowel(transient)

due to mesenteric artery insufficiency

K55.1

Syndrome

IVC(intravascular coagulopathy)

D65

Syndrome

Jaccoud's

See: Arthropathy, postrheumatic, chronic

Syndrome

Jakob-Creutzfeldt

See: Creutzfeldt-Jakob disease or syndrome

Syndrome

Jervell-Lange-Nielsen

I45.81

Syndrome

Joseph-Diamond-Blackfan

D61.01

Syndrome

jugular foramen

G52.7

Syndrome

Kabuki(type 1, due to KMT2D mutation) (type 2, due to KDM6A mutation)

Q89.81

Syndrome

Kanner's(autism)

F84.0

Syndrome

Kartagener's

Q89.3

Syndrome

Kimmelstiel-Wilson

See: Diabetes, specified type, with Kimmelstiel-Wilson disease

Syndrome

Klippel-Feil(brevicollis)

Q76.1

Syndrome

Köhler-Pellegrini-Stieda

See: Bursitis, tibial collateral

Syndrome

Korsakoff(-Wernicke) (nonalcoholic)

F04

Syndrome › Korsakoff(-Wernicke) (nonalcoholic)

alcoholic

F10.26

Syndrome

Krabbe's congenital muscle hypoplasia

Q79.8

Syndrome

labyrinthine

Subcategory: H83.2

Syndrome › Lambert-Eaton

in

Syndrome › Lambert-Eaton › in

neoplastic disease

G73.1

Syndrome › Lambert-Eaton › in

specified disease NEC

G70.81

Syndrome

Landau-Kleffner

See: Epilepsy, specified NEC

Syndrome

Lassueur Graham-Little Piccardi

L66.19

Syndrome

lateral

Syndrome › lateral

cutaneous nerve of thigh

G57.1-

Syndrome › lateral

medullary

G46.4

Syndrome

lazy

Syndrome › lazy

leukocyte

D70.8

Syndrome › lazy

posture

M62.3

Syndrome › Lennox-Gastaut

intractable

G40.814

Syndrome › Lennox-Gastaut › intractable

with status epilepticus

G40.813

Syndrome › Lennox-Gastaut › intractable

without status epilepticus

G40.814

Syndrome › Lennox-Gastaut

not intractable

G40.812

Syndrome › Lennox-Gastaut › not intractable

with status epilepticus

G40.811

Syndrome › Lennox-Gastaut › not intractable

without status epilepticus

G40.812

Syndrome

lenticular, progressive

E83.01

Syndrome

Lignac(de Toni) (-Fanconi) (-Debré)

E72.09

Syndrome › Lignac(de Toni) (-Fanconi) (-Debré)

with cystinosis

E72.04

Syndrome

limbic epilepsy personality

F07.0

Syndrome

liver-kidney

K76.7

Syndrome

long arm 18 or 21 deletion

Q93.89

Syndrome

Louis-Barré

G11.3

Syndrome

low

Syndrome › low

atmospheric pressure

T70.29

Syndrome › low

output(cardiac)

I50.9

Syndrome

lower radicular, newborn(birth injury)

P14.8

Syndrome

Luetscher's(dehydration)

E86.0

Syndrome

Lupus anticoagulant

D68.62

Syndrome

macrophage activation

D76.1

Syndrome › macrophage activation

due to infection

D76.2

Syndrome

magnesium-deficiency

R29.0

Syndrome

Mal de Debarquement

R42

Syndrome

malabsorption

K90.9

Syndrome › malabsorption

postsurgical

K91.2

Syndrome

malformation, congenital, due to

Syndrome › malformation, congenital, due to

alcohol

Q86.0

Syndrome › malformation, congenital, due to

exogenous cause NEC

Q86.8

Syndrome › malformation, congenital, due to

hydantoin

Q86.1

Syndrome › malformation, congenital, due to

warfarin

Q86.2

Syndrome

malignant

Syndrome › malignant

carcinoid

E34.00

Syndrome › malignant

neuroleptic

G21.0

Syndrome

Mallory-Weiss

K22.6

Syndrome

mandibulofacial dysostosis

Q75.4

Syndrome

manic-depressive

See: Disorder, bipolar

Syndrome

maple-syrup-urine

E71.0

Syndrome › Marfan

with

Syndrome › Marfan › with

cardiovascular manifestations

Q87.418

Syndrome › Marfan › with › cardiovascular manifestations

aortic dilation

Q87.410

Syndrome › Marfan › with

ocular manifestations

Q87.42

Syndrome › Marfan › with

skeletal manifestations

Q87.43

Syndrome

Marie's(acromegaly)

E22.0

Syndrome

mast cell activation

See: Activation, mast cell

Syndrome

maternal hypotension

See: Syndrome, hypotension, maternal

Syndrome

May(-Hegglin)

D72.0

Syndrome

McArdle(-Schmidt) (-Pearson)

E74.04

Syndrome

meconium plug(newborn)

P76.0

Syndrome

MED13L(mediator complex subunit 13L)

Q87.85

Syndrome

median arcuate ligament

I77.4

Syndrome

mediator complex subunit 13L(MED13L)

Q87.85

Syndrome

Meekeren-Ehlers-Danlos

Q79.6

Syndrome

megavitamin-B6

E67.2

Syndrome

MERRF(myoclonic epilepsy associated with ragged-red fibers)

E88.42

Syndrome

mesenteric

Syndrome › mesenteric

artery(superior)

K55.1

Syndrome › mesenteric

vascular insufficiency

K55.1

Syndrome

metastatic carcinoid

E34.00

Syndrome

micrognathia-glossoptosis

Q87.0

Syndrome

middle lobe(lung)

J98.19

Syndrome

middle radicular

G54.0

Syndrome

migraine

G43.909-

See also: Migraine