MeSH Browser

MeSH Supplementary: Optic atrophy, X-linked
Unique ID: C537125
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537125
Entry Term(s): Optic atrophy 2; Optic atrophy, non-Leber type, with early onset
Registry Numbers: 0
Heading Mapped to: Optic Atrophy / congenital; *Genetic Diseases, X-Linked
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Optic atrophy, X-linked MeSH Supplementary Concept Data 2025