OBO ID: DOID:0080287
Term Name: spinocerebellar ataxia 45 Search Ontology:
Synonyms:
Definition: An autosomal dominant cerebellar ataxia that has_material_basis_in heterozygous mutation in the FAT2 gene on chromosome 5q33. https://pubmed.ncbi.nlm.nih.gov/29053796/
References:
Ontology: Human Disease   ( DOID:0080287 )
Relationships
is a type of:
OTHER spinocerebellar ataxia 45 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FAT2 Spinocerebellar ataxia 45 617769
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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