Cataract, Congenital Nuclear, Autosomal Recessive 2 MeSH Supplementary Concept Data 2024

Details
Concepts

MeSH Supplementary: Cataract, Congenital Nuclear, Autosomal Recessive 2
Unique ID: C565725
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565725
Entry Term(s): CATCN2
Registry Number: 0
Heading Mapped to: *Cataract; *Eye Diseases, Hereditary
Frequency: 0
Date of Entry: 2012/11/05

Cataract, Congenital Nuclear, Autosomal Recessive 2 Preferred

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