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DOID:0060194 - amyotrophic lateral sclerosis type 2
Disease Ontology Definition:An amyotrophic lateral sclerosis that has material basis in mutation in the alsin gene on chromosome 2.
Synonyms: ALS2, amyotrophic lateral sclerosis 2, amyotrophic lateral sclerosis 2, juvenile,
Echinobase Genes : als2
MIM:205100 - amyotrophic lateral sclerosis 2, juvenile; als2 |
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)