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Summary Literature (0)
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 Disease Ontology (on Monarch Initiative):
MONDO:0013264 - amyotrophic lateral sclerosis type 12


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)