ZFIN Human Disease: autosomal recessive spinocerebellar ataxia 26

OBO ID: DOID:0080260

OBO ID: DOID:0080260

Term Name:	autosomal recessive spinocerebellar ataxia 26	Search Ontology:
Synonyms:	SCAR26
Definition:	An autosomal recessive cerebellar ataxia that has_material_basis_in compound heterozygous mutation in the XRCC1 gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/28002403
References:	OMIM:617633
Ontology:	Human Disease ( DOID:0080260 )

Relationships

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

OTHER autosomal recessive spinocerebellar ataxia 26 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
XRCC1	xrcc1	?Spinocerebellar ataxia, autosomal recessive 26	617633

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None