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Echinobase
Summary Literature (0)
DOID:0050556 - infantile onset spinocerebellar ataxia

Disease Ontology Definition:n_a

Synonyms: OHAHA SYNDROME,

Echinobase Genes : twnk


OMIM:
MIM:271245 - mitochondrial dna depletion syndrome 7 (hepatocerebral type); mtdps7

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

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