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DOID:0050556 - infantile onset spinocerebellar ataxia
Disease Ontology Definition:n_a
Synonyms: OHAHA SYNDROME,
Echinobase Genes : twnk
MIM:271245 - mitochondrial dna depletion syndrome 7 (hepatocerebral type); mtdps7 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal recessive cerebellar ataxia (is_a)