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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,
Xenbase Genes
:
pon2,
prph,
hnrnpa1,
fus,
erbb4,
nefh,
als2,
optn,
chmp2b,
tbk1,
anxa11,
ccnf,
setx,
vcp,
cfap410,
| MONDO:0004976 - amyotrophic lateral sclerosis |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
monogenic disease (is_a),
motor neuron disease (is_a)