You are using an outdated browser. Please upgrade your browser to improve your experience.
myopathy caused by varation in POMT2
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Any myopathy in which the cause of the disease is a variation in the POMT2 gene.
Mondo Term and Equivalent IDs
MONDO:0700071: myopathy caused by varation in POMT2
Use Cases
Submit Feedback
Download Data for myopathy caused by varation in POMT2
data still loading...
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
MONDO:0700071
High level summary of knowledge for a disease, including descriptions and datasource references.