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Optic atrophy and cataract, autosomal dominant MeSH Supplementary Concept Data 2024


MeSH Supplementary
Optic atrophy and cataract, autosomal dominant
Unique ID
C537128
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C537128
Entry Term(s)
Opa3, Autosomal Dominant
Optic Atrophy 3, Autosomal Dominant
Optic atrophy, cataract, and neurologic disorder
Heading Mapped to
Cataract / congenital
*Optic Atrophies, Hereditary
Frequency
0
Date of Entry
2010/08/25
Revision Date
2013/11/06
Optic atrophy and cataract, autosomal dominant Preferred
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