MeSH Browser

MeSH Supplementary: Moyamoya disease 1
Unique ID: C536991
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536991
Entry Term(s): MYMY1; Spontaneous occlusion of the circle of Willis
Registry Numbers: 0
Heading Mapped to: *Moyamoya Disease
Frequency: 191
Note: A hereditary autosomal recessive form of Moyamoya disease. Susceptibility has been mapped to chromosome 3. OMIM: 252350
Date of Entry: 2010/08/25
Revision Date: 2015/08/18

Moyamoya disease 1 MeSH Supplementary Concept Data 2025