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DO Term : CADASIL 1 [DOID:0111035] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A CADASIL characterized by migraine, strokes, and white matter lesions that has_material_basis_in heterozygous mutation in the NOTCH3 gene on chromosome 19p13.
  • synonyms:
  • autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1,
  • 125310,
  • OMIM:125310,
  • ICD10CM:F01.1
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Disease

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Ontology

Ontology Term --> All ancestors

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Ontology Term --> Direct parents





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