ZFIN Human Disease: autosomal recessive spinocerebellar ataxia 24

OBO ID: DOID:0111615

Term Name:	autosomal recessive spinocerebellar ataxia 24		Search Ontology:
Synonyms:	SCAR24
Definition:	An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the UBA5 gene on chromosome 3q22.1. https://www.ncbi.nlm.nih.gov/pubmed/26872069
References:	OMIM:617133
Ontology:	Human Disease ( DOID:0111615 )

Relationships

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

OTHER autosomal recessive spinocerebellar ataxia 24 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
UBA5	uba5	?Spinocerebellar ataxia, autosomal recessive 24	617133

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None