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Summary Literature (0)
DOID:0111036 - CADASIL 2

Disease Ontology Definition:A CADASIL characterized by stroke, transient ischemic attacks, cognitive impairment, dementia, balance impairment, gait disturbance, headaches, and/or seizures associated with early confluent or confluent diffuse white matter hyperintensities that has_material_basis_in heterozygous mutation in the HTRA1 gene on chromosome 10q26.

Synonyms: autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 2

Xenbase Genes : htra1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014768 - superior palpebral vein


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), CADASIL (is_a)