ZFIN Human Disease: autosomal recessive spinocerebellar ataxia 17

OBO ID: DOID:0080064

OBO ID: DOID:0080064

Term Name:	autosomal recessive spinocerebellar ataxia 17	Search Ontology:
Synonyms:	SCAR17
Definition:	An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the CWF19L1 gene on chromosome 10q24. https://www.ncbi.nlm.nih.gov/pubmed/26197978
References:	OMIM:616127
Ontology:	Human Disease ( DOID:0080064 )

Relationships

is a type of:	autosomal recessive cerebellar ataxia autosomal recessive cerebellar ataxia Show first 5 Terms

OTHER autosomal recessive spinocerebellar ataxia 17 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CWF19L1	cwf19l1	Spinocerebellar ataxia, autosomal recessive 17	616127

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None