OBO ID: DOID:0050958
Term Name: spinocerebellar ataxia type 7 Search Ontology:
Synonyms:
Definition: An autosomal dominant cerebellar ataxia that is characterized by ataxia, progressive vision loss, and failure to thrive, has_material_basis_in mutation in the ATXN7 gene. https://rarediseases.info.nih.gov/diseases/4955/spinocerebellar-ataxia-7
References:
Ontology: Human Disease   ( DOID:0050958 )
OTHER spinocerebellar ataxia type 7 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ATXN7 Spinocerebellar ataxia 7 164500
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None