spastic ataxia 5

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Summary

Literature (0)

DOID:0050944 - spastic ataxia 5

Disease Ontology Definition:A spastic ataxia that is characterized by early onset of cerebellar ataxia, spasticity, oculomotor apraxia, dystonia and myoclonic epilepsy, has_material_basis_in homozygous mutation in the AFG3L2 gene on chromosome 18p11.

Synonyms:

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: afg3l2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013776 - spastic ataxia 5

MONDO:0013776 - spastic ataxia 5

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), spastic ataxia (is_a)