Cataract, Congenital Nuclear, Autosomal Recessive 3 MeSH Supplementary Concept Data 2024

Details
Concepts

MeSH Supplementary: Cataract, Congenital Nuclear, Autosomal Recessive 3
Unique ID: C566923
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566923
Entry Term(s): CATCN3
Heading Mapped to: *Cataract; *Eye Diseases, Hereditary
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Cataract, Congenital Nuclear, Autosomal Recessive 3 Preferred

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