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Cataract, Autosomal Dominant, Multiple Types 1 MeSH Supplementary Concept Data 2024


MeSH Supplementary
Cataract, Autosomal Dominant, Multiple Types 1
Unique ID
C566909
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C566909
Registry Number
0
Heading Mapped to
*Cataract
Frequency
0
Note
mutation on phakinin
Date of Entry
2012/11/05
Cataract, Autosomal Dominant, Multiple Types 1 Preferred
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