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 (1)
DOID:332 - amyotrophic lateral sclerosis


Disease Ontology Definition:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing.

Synonyms: ALS, Lou Gehrig's disease, motor neuron disease, bulbar


In Mondo Disease Ontology:
MONDO:0004976 - amyotrophic lateral sclerosis

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : pon2, prph, hnrnpa1, fus, erbb4, nefh, als2, optn, chmp2b, tbk1, anxa11, ccnf, setx, vcp, cfap410, [+]

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): monogenic disease (is_a), motor neuron disease (is_a)