Cataract, Autosomal Dominant Nuclear MeSH Supplementary Concept Data 2024

Details
Concepts

MeSH Supplementary: Cataract, Autosomal Dominant Nuclear
Unique ID: C565137
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565137
Registry Number: 0
Heading Mapped to: Cataract / *congenital
Frequency: 12
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Cataract, Autosomal Dominant Nuclear Preferred

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