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DOID:0060208 - amyotrophic lateral sclerosis type 17
Disease Ontology Definition:An amyotrophic lateral sclerosis that has material basis in mutation in the CHMP2B gene on chromosome 3.
Synonyms: ALS17, CHMP2B-related amyotrophic lateral sclerosis, amyotrophic lateral sclerosis 17,
Echinobase Genes :
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
amyotrophic lateral sclerosis (is_a)