You are using an outdated browser. Please upgrade your browser to improve your experience.
factor XIII deficiency
Disease Summary
Associated Targets (2)
Tchem
1
Tbio
1
Mondo Description An acquired or inherited coagulation disorder due to reduced levels and activity of factor XIII.
Mondo Term and Equivalent IDs
MONDO:0002241: factor XIII deficiency
Use Cases
Submit Feedback
Download Data for factor XIII deficiency
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:0002241
High level summary of knowledge for a disease, including descriptions and datasource references.