CADASIL 1

Term ID

DOID:0111035

Synonyms

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

Definition

A CADASIL characterized by migraine, strokes, and white matter lesions that has_material_basis_in heterozygous mutation in the NOTCH3 gene on chromosome 19p13. (2)

References

• ICD10CM:F01.1
• OMIM:125310

Ontology

Human Disease   ( DOID:0111035 )