MeSH Browser

MeSH Supplementary: Behr syndrome
Unique ID: C537669
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537669
Entry Term(s): Optic Atrophy, Infantile Hereditary, With Neurologic Abnormalities; Optic atrophy, infantile hereditary, Behr complicated form of
Heading Mapped to: *Ataxia; *Intellectual Disability; Optic Atrophy / congenital; *Spasm; *Hearing Loss
Frequency: 16
Note: Optic atrophy in early childhood, associated with ataxia, spasticity, mental retardation, and posterior column sensory loss
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Behr syndrome MeSH Supplementary Concept Data 2024