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MIM:616779 - CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2; CADASIL2
Xenbase Genes: htra1
Human Disease Resource: MIM
MONDO:0014768 - superior palpebral vein |
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MONDO:0014768 - superior palpebral vein |