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:913 - atrophic muscular disease

Disease Ontology Definition:A neuromuscular disease that is characterized by an abnormal reduction in the muscle volume and atrophy.

Synonyms:

Xenbase Genes : popdc1, syne2, flnc, hnrnpdl, dmd.2, cnbp, lmna, gmppb, sgcb, pomt1, sgcd, dmpk, lama2, tor1aip1, emd, [+]

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0004714 - septum pellucidum


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): muscular disease (is_a), neuromuscular disease (is_a)