ZFIN Human Disease: autosomal recessive spinocerebellar ataxia 11

OBO ID: DOID:0080063

OBO ID: DOID:0080063

Term Name:	autosomal recessive spinocerebellar ataxia 11	Search Ontology:
Synonyms:	SCAR11
Definition:	An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the SYT14 gene on chromosome 1q32. https://www.ncbi.nlm.nih.gov/pubmed/21835308
References:	OMIM:614229
Ontology:	Human Disease ( DOID:0080063 )

Relationships

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

OTHER autosomal recessive spinocerebellar ataxia 11 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SYT14	syt14a	?Spinocerebellar ataxia, autosomal recessive 11	614229

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None