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DOID:0060204 - amyotrophic lateral sclerosis type 13
Disease Ontology Definition:An amyotrophic lateral sclerosis where a mutation that has material basis in the ATXN2 gene on chromosome 12 contributes to suscepitbility.
Synonyms: ALS13, amyotrophic lateral sclerosis 13,
Xenbase Genes :
MONDO:0008458 - spinocerebellar ataxia type 2 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
amyotrophic lateral sclerosis (is_a)