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MIM:600142 - CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CARASIL
Xenbase Genes: htra1
Human Disease Resource: MIM
MONDO:0010829 - CARASIL syndrome |
DOID:13945 - CADASIL |
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MONDO:0010829 - CARASIL syndrome |
DOID:13945 - CADASIL |