Search Ontology:
Human Disease

X-linked spinocerebellar ataxia 4

Term ID
DOID:0111832
Synonyms
  • SCAX4
  • X-linked ataxia-dementia syndrome
  • X-linked spinocerebellar ataxia type 4
Definition
An X-linked cerebellar ataxia characterized by ataxia, pyramidal tract signs and adult-onset dementia with X-linked inheritance. https://www.ncbi.nlm.nih.gov/pubmed/3470628
References
Ontology
Human Disease   ( DOID:0111832 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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