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Cataract, Autosomal Dominant MeSH Supplementary Concept Data 2024


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 Number
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 Preferred
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