MeSH Browser

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
Registry Number: 0
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 MeSH Supplementary Concept Data 2024