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Download Data for familial dysfibrinogenemia
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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.
This disease has been annotated by GARD as a rare disease.
Description from Mondo Disease Ontology.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
GARD:0002004
NCIT:C131659
OMIM:616004
Orphanet:98881
SCTID:111589005
UMLS:C1260903
UMLS:CN207171
MONDO:0014452
High level summary of knowledge for a disease, including descriptions and datasource references.
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Opens the Target List with this set of targets