- OMIM ID
-
600142
- OMIM term:
- CEREBRAL AUTOSOMAL RECESSIVE ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CARASIL
- Alternative terms:
-
MAEDA SYNDROME
SUBCORTICAL VASCULAR ENCEPHALOPATHY, PROGRESSIVE
CEREBROVASCULAR DISEASE WITH THIN SKIN, ALOPECIA, AND DISC DISEASE
- (∗) Location:
- 10q26.13
- (†) Associated OMIM genes:
- HTRA1
- (‡) Associated MGI genes:
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