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Summary Literature (0)
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

Xenbase Genes : als2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008780 - inner cell mass derived epiblast

MIM:
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
Parent(s): amyotrophic lateral sclerosis (is_a)