MeSH Browser

MeSH Supplementary: Costeff optic atrophy syndrome
Unique ID: C535311
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535311
Entry Term(s): 3-methylglutaconic aciduria, type III; Costeff syndrome; Iraqi Jewish optic atrophy plus; OPA3, Autosomal Recessive; Optic Atrophy 3, Autosomal Recessive; Optic atrophy plus syndrome; Optic atrophy, infantile, with chorea and spastic paraplegia
Registry Number: 0
Heading Mapped to: *Chorea; *Metabolism, Inborn Errors; *Optic Atrophy; *Spastic Paraplegia, Hereditary
Frequency: 12
Date of Entry: 2010/08/25
Revision Date: 2012/08/24

Costeff optic atrophy syndrome MeSH Supplementary Concept Data 2024