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Summary Literature (0)
DOID:0060211 - amyotrophic lateral sclerosis type 20

Disease Ontology Definition:An amyotrophic lateral sclerosis with juvenile onset that has_material_basis_in mutation in the HNRNPA1 gene on chromosome 12.

Synonyms: ALS20, amyotrophic lateral sclerosis 20

Xenbase Genes : hnrnpa1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014181 - amyotrophic lateral sclerosis type 20

MIM:
MIM:615426 - AMYOTROPHIC LATERAL SCLEROSIS 20; ALS20

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)