Cataract, Autosomal Dominant [Supplementary Concept]
Hereditary forms of cataract caused by mutations in the CRYAA gene. OMIM: 604219
Date introduced: November 5, 2012
MeSH Unique ID: C565815
Heading Mapped to:
Entry Terms:
- Cataract 9, Multiple Types
- Cataract 9, multiple types, with or without microcornea