loading...| Preferred Name | pulmonary arterial hypertension | |
| Synonyms |
PPH idiopathic pulmonary hypertension PAH |
|
| Definitions |
Pulmonary arterial hypertension (PAH) is a group of diseases characterized by elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, or induced by drug or toxin (drug-or toxin-induced PAH) or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease). |
|
| ID |
http://purl.obolibrary.org/obo/MONDO_0015924 |
|
| closeMatch | ||
| database_cross_reference |
MedDRA:10064911 SCTID:11399002 Orphanet:182090 UMLS:C2973725 GARD:0007501 UMLS:CN200519 |
|
| exactMatch |
http://identifiers.org/meddra/10064911 http://linkedlifedata.com/resource/umls/id/C0152171 http://linkedlifedata.com/resource/umls/id/CN200519 http://www.orpha.net/ORDO/Orphanet_182090 http://identifiers.org/snomedct/11399002 |
|
| has exact synonym |
PAH |
|
| has modifier | ||
| has related synonym |
PPH idiopathic pulmonary hypertension |
|
| id |
MONDO:0015924 |
|
| imported from | ||
| in_subset |
http://purl.oboInOwllibrary.org/oboInOwl/mondo#ordo_group_of_disorders |
|
| label |
pulmonary arterial hypertension |
|
| notation |
MONDO:0015924 |
|
| prefLabel |
pulmonary arterial hypertension |
|
| textual definition |
Pulmonary arterial hypertension (PAH) is a group of diseases characterized by elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, or induced by drug or toxin (drug-or toxin-induced PAH) or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease). |
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| subClassOf |