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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,
Echinobase Genes :
MIM:615426 - amyotrophic lateral sclerosis 20; als20 |
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)