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Download Data for familial hypofibrinogenemia
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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.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
GARD:0002887
Orphanet:101041
UMLS:CN197419
MONDO:0015096
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