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Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy MeSH Supplementary Concept Data 2026


MeSH Supplementary
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
Unique ID
C563990
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C563990
Entry Term(s)
CARASIL
Cerebrovascular Disease with Thin Skin, Alopecia, and Disc Disease
Familial Young-Adult-Onset Arteriosclerotic Leukoencephalopathy with Alopecia and Lumbago without Arterial Hypertension
MAEDA Syndrome
Nemoto Disease
Subcortical Vascular Encephalopathy, Progressive
Registry Numbers
0
Heading Mapped to
*Alopecia
*Cerebral Infarction
*Spinal Diseases
*Leukoencephalopathies
Frequency
51
Note
A hereditary autosomal recessive nonhypertensive cerebral small vessel arteriopathy characterized by alopecia, SPONDYLOSIS, and progressive motor dysfunction and DEMENTIA with onset typically in the second or third decade of life. Mutations in the HTRA1 gene have been identified. OMIM: 600142
Date Introduced
2012/11/05
Last Updated
2015/08/18
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Preferred
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