ZFIN Human Disease: spinocerebellar ataxia type 37

OBO ID: DOID:0050984

OBO ID: DOID:0050984

Term Name:	spinocerebellar ataxia type 37	Search Ontology:
Synonyms:
Definition:	An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia and dysarthria, presenting in mid-adulthood, and has_material_basis_in mutation to the DAB1 gene. https://www.omim.org/entry/615945
References:	OMIM:615945
Ontology:	Human Disease ( DOID:0050984 )

Relationships

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

OTHER spinocerebellar ataxia type 37 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
DAB1	dab1b dab1a	Spinocerebellar ataxia 37	615945

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS (1)