|
DOID:0080102 - congenital fiber-type disproportion
Disease Ontology Definition:n_a
Synonyms:
Echinobase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MIM:255310 - myopathy, congenital, with fiber-type disproportion; cftd |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
congenital myopathy (is_a)