Search Ontology:
Human Disease

X-linked spinocerebellar ataxia 2

Term ID
DOID:0111830
Synonyms
  • cerebellar ataxia with extrapyramidal involvement early-onset
  • SCAX2
Definition
An X-linked cerebellar ataxia characterized by infantile onset of ataxia, severe atrophy of the cerebellum, diffuse small cysts, pale inferior olives, and gliosis with X-linked inheritance. https://www.ncbi.nlm.nih.gov/pubmed/13541590
References
Ontology
Human Disease   ( DOID:0111830 )
Relationships
is a type of
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Genes Involved
Zebrafish Models