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DOID:0060203 - amyotrophic lateral sclerosis type 12
Disease Ontology Definition:An amyotrophic lateral sclerosis that has_material_basis_in mutation in the OPTN gene on chromosome 10.
Synonyms: ALS12, amyotrophic lateral sclerosis 12
Xenbase Genes : optn
MONDO:0013264 - amyotrophic lateral sclerosis type 12 |
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)