Infantile onset spinocerebellar ataxia [Supplementary Concept]
mutation in C10ORF2
Date introduced: August 25, 2010
MeSH Unique ID: C535523
Heading Mapped to:
Entry Terms:
- Infantile-Onset Spinocerebellar Ataxia
- Ophthalmoplegia, hypotonia, ataxia, hypacusis, and athetosis
- Spinocerebellar ataxia infantile with sensory neuropathy
- Spinocerebellar Ataxia, Infantile, with Sensory Neuropathy
- OHAHA Syndrome