amyotrophic lateral sclerosis type 2

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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

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: als2

MIM:

MIM:205100 - amyotrophic lateral sclerosis 2, juvenile; als2

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, Ontobee

Parent(s): amyotrophic lateral sclerosis (is_a)