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Disease index

Syndrome

Disease index · Modifiers and references

Modifiers and references · icd10cm-index-2027.xml

Syndrome

hyperkinetic

See: Hyperkinesia

Syndrome

hypermobility

M35.7

Syndrome

hypernatremia

E87.0

Syndrome

hyperosmolarity(see also, Diabetes, by type, with hyperosmolarity)

E87.0

Syndrome

hypersplenic

D73.1

Syndrome

hypertransfusion, newborn

P61.1

Syndrome

hyperventilation

F45.8

Syndrome

hyperviscosity( of serum)

Syndrome › hyperviscosity( of serum)

polycythemic

D75.1

Syndrome › hyperviscosity( of serum)

sclerothymic

D58.8

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

inherited neoplasm predisposition syndrome of multiple systems, specified NEC

QA1.798

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

F10.9-

Syndrome › Korsakoff(-Wernicke) (nonalcoholic) › alcoholic

with dependence

F10.2-

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

Lynch(due to EPCAM) (due to MLH1) (due to MSH2) (due to MSH6) (due to PMS2)

QA1.71

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