|
DOID:0050970 - spinocerebellar ataxia type 19/22
Disease Ontology Definition:n_a
Synonyms:
OMIM:607346 - SPINOCEREBELLAR ATAXIA 19; SCA19 |
MONDO:0011819 - spinocerebellar ataxia type 19/22 |
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s):
autosomal dominant cerebellar ataxia (is_a)