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:0111072 - myostatin-related muscle hypertrophy

Disease Ontology Definition:A muscle tissue disease characterized by increased muscle bulk and strength that has_material_basis_in homozygous mutation in the MSTN gene on chromosome 2q32.2.

Synonyms: MSLHP

Xenbase Genes : mstn, mstn.2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013598 - myostatin-related muscle hypertrophy

MIM:
MIM:614160 - MUSCLE HYPERTROPHY; MSLHP

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

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