ZFIN Human Disease: autosomal recessive spinocerebellar ataxia 10

OBO ID: DOID:0050999

Term Name:	autosomal recessive spinocerebellar ataxia 10		Search Ontology:
Synonyms:	SCAR10
Definition:	An autosomal recessive cerebellar ataxia that is characterized by ataxia, dysarthria, nystagmus and marked cerebellar atrophy, has_material_basis_in mutation in the ANO10 gene. https://www.omim.org/entry/613728
References:	OMIM:613728
Ontology:	Human Disease ( DOID:0050999 )

Relationships

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

OTHER autosomal recessive spinocerebellar ataxia 10 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
ANO10	ano10a ano10b	Spinocerebellar ataxia, autosomal recessive 10	613728

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None