MeSH Browser

MeSH Supplementary: Alpha-B Crystallinopathy
Unique ID: C563848
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563848
Entry Term(s): Myopathy, Cardioskeletal, Desmin-Related, with Cataract; Myopathy, Desmin-Related, associated with Mutation in the CRYAB Gene; Myopathy, Myofibrillar, Alpha-B Crystallin-Related
Registry Numbers: 0
Heading Mapped to: *Cataract; *Muscular Diseases; *Cardiomyopathies
Frequency: 3
Note: mutation in CRYAB
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Alpha-B Crystallinopathy MeSH Supplementary Concept Data 2025