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DO Term : CADASIL [DOID:13945] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A leukodystrophy characterized by recurrent subcortical ischemic stroke and cognitive impairment.

synonyms:
OMIM:600142,
cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy,
MESH:D046589,
SNOMEDCT_US_2023_03_01:390723008,
hereditary multi-infarct dementia,
600142,
PS125310,
NCI:C84606,
OMIM:PS125310,
ICD10CM:I67.850,
ORDO:136,
UMLS_CUI:C0751587,
GARD:1049

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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