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


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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