ZFIN Human Disease: autosomal recessive spinocerebellar ataxia 25

OBO ID: DOID:0080259

OBO ID: DOID:0080259

Term Name:	autosomal recessive spinocerebellar ataxia 25	Search Ontology:
Synonyms:	SCAR25
Definition:	An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the ATG5 gene on chromosome 6q21. https://www.ncbi.nlm.nih.gov/pubmed/26812546
References:	OMIM:617584
Ontology:	Human Disease ( DOID:0080259 )

Relationships

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

OTHER autosomal recessive spinocerebellar ataxia 25 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
ATG5	atg5	?Spinocerebellar ataxia, autosomal recessive 25	617584

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None