autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1 Disease Ontology Browser

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Disease Ontology Browser

autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1 (DOID:0061227)
Alliance: disease page
Alt IDs: OMIM:621295
Definition: A CADASIL characterized by the onset of neurologic symptoms in infancy or early childhood that has_material_basis_in homozygous or compound heterozygous mutations in the NOTCH3 gene on chromosome 19p13.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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