Cataract, Autosomal Dominant, Multiple Types 1 MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Cataract, Autosomal Dominant, Multiple Types 1
Unique ID: C566909
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566909
Registry Numbers: 0
Heading Mapped to: *Cataract
Frequency: 0
Note: mutation on phakinin
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Cataract, Autosomal Dominant, Multiple Types 1 Preferred

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