Disease & disorder

cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1

MONDO:0000914

A CADASIL characterized by migraine, strokes, and white matter lesions that has material basis in heterozygous mutation in the NOTCH3 gene on chromosome 19p13.

Outbreak surveillance

Global reported events

Explore recent public health notices potentially related to cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1. Results are keyword matches, not yet verified disease-to-outbreak relationships.

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Clinical trials0
Recruiting0
Drug concepts studied0
Synonyms13
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Background context

cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1

Wikidata Q32146322 ↗
Background only. Canonical identity remains MONDO; clinical-trial relationships come from ClinicalTrials.gov.

Drugs being studied

Disease identity and terminology: MONDO. Trial relationships: ClinicalTrials.gov.