CARASIL syndrome
https://github.com/monarch-initiative/mondo/issues/6752
cerebrovascular disease with thin skin, alopecia, and disk disease
Orphanet:199354
SCTID:703219008
MESH:C563990
cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy
CARASIL
CARASIL is a hereditary cerebral small vessel disease characterized by early-onset gait disturbances, premature scalp alopecia, ischemic stroke, acute mid to lower back pain and progressive cognitive disturbances leading to severe dementia.
cerebrovascular disease with thin skin, alopecia, and disc disease
MONDO:0010829
NORD:888
UMLS:C1838577
subcortical vascular encephalopathy, progressive
OMIM:600142
Maeda syndrome
GARD:10424
cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2