MeSH Browser

MeSH Supplementary: Cataract, Autosomal Dominant
Unique ID: C565815
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565815
Entry Term(s): Cataract 9, Multiple Types; Cataract 9, multiple types, with or without microcornea
Registry Numbers: 0
Heading Mapped to: *Cataract
Frequency: 50
Note: Hereditary forms of cataract caused by mutations in the CRYAA gene. OMIM: 604219
Date of Entry: 2012/11/05
Revision Date: 2015/09/25

Cataract, Autosomal Dominant MeSH Supplementary Concept Data 2025