CADASIL - [cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy] syndrome

Description

CADASIL is the acronym for Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy. CADASIL is a genetic disease transmitted in an autosomal dominant pattern. It is associated with ischemic stroke, migraine, dementia, psychological disturbances.

Index terms

CADASIL - [cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy] syndrome
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy syndrome

Exclusions from above levels

8B25 – Late effects of cerebrovascular disease
NA07 – Intracranial injury
05 – Endocrine, nutritional or metabolic diseases

Show allHide

18 – Complications of pregnancy, childbirth and the puerperium
19 – Certain conditions originating in the perinatal period
22 – Injury, poisoning or certain other consequences of external causes

Sibling codes

8B22.C1 – CARASIL - [cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy] syndrome
8B22.CY – Other specified hereditary cerebrovascular diseases
8B22.CZ – Hereditary cerebrovascular diseases, unspecified

Foundation entity

CADASIL - [cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy] syndrome – http://id.who.int/icd/entity/1621899838

Allowed postcoordination axes

hasManifestation

Part of: 8B22.C: Hereditary cerebrovascular diseases › 8B22: Certain specified cerebrovascular diseases › 08: Diseases of the nervous system