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idiopathic pulmonary arterial hypertension
Disease Summary
Associated Targets (20)
Tbio
11
Tclin
5
Tchem
4
Mondo Description Idiopathic pulmonary arterial hypertension (IPAH) is a sporadic form of pulmonary arterial hypertension (PAH) characterized by elevated pulmonary arterial resistance leading to right heart failure. IPAH is progressive and potentially fatal and not associated with an underlying condition or family history of PAH.
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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.
Description from Mondo Disease Ontology.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
ICD9:416.0
Orphanet:275766
SCTID:697898008
UMLS:C3203102
UMLS:CN202574
MONDO:0017147
High level summary of knowledge for a disease, including descriptions and datasource references.