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Summary Literature (0)
DOID:0050969 - spinocerebellar ataxia type 18

Disease Ontology Definition:An autosomal dominant cerebellar ataxia that is characterized by cerebellar ataxia and sensory neuropathy, has_material_basis_in mutation on chromosome 7q22-q23.

Synonyms:

Xenbase Genes : ifrd1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011834 - spinocerebellar ataxia type 18


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant cerebellar ataxia (is_a)