MeSH Browser

MeSH Supplementary: Optic atrophy 6
Unique ID: C537127
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537127
Entry Term(s): Optic atrophy, congenital or early infantile, autosomal recessive
Registry Number: 0
Heading Mapped to: *Optic Atrophies, Hereditary
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Optic atrophy 6 MeSH Supplementary Concept Data 2024