Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0060193 - amyotrophic lateral sclerosis type 1

Disease Ontology Definition:An amyotrophic lateral sclerosis that has_material_basis_in mutation in the SOD1 gene on chromosome 21. The most common type of familial ALS.

Synonyms: ALS1, amyotrophic lateral sclerosis 1,

Xenbase Genes : prph, nefh, sod1, dctn1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007103 - amyotrophic lateral sclerosis type 1


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), autosomal dominant disease (is_a), autosomal recessive disease (is_a)