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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

Referenced OMIM:

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
Parent(s): monogenic disease (is_a), motor neuron disease (is_a)


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