CARASIL syndrome https://github.com/monarch-initiative/mondo/issues/6752 https://www.malacards.org/card/cerebral_arteriopathy_autosomal_recessive_with_subcortical_infarcts_and_leukoencephalopathy cerebrovascular disease with thin skin, alopecia, and disk disease icd11.foundation:984450655 Orphanet:199354 SCTID:703219008 MESH:C563990 cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy GARD:0010424 MEDGEN:325051 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 NANDO:1200544 subcortical vascular encephalopathy, progressive DOID:0061228 OMIM:600142 Maeda syndrome cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2