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
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes : prph, hnrnpa1, fus, erbb4, nefh, als2, tbk1, setx, tardbp, matr3, sod1, pfn1, sigmar1, c9orf72, sqstm1,
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD