|
DOID:0050556 - infantile onset spinocerebellar ataxia
Disease Ontology Definition:n_a
Synonyms: OHAHA SYNDROME,
Echinobase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
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)