eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | idiopathic pulmonary arterial hypertension |
| Comorbidity | C1619734|pulmonary arterial hypertension |
| Sentences | 3 |
| PubMedID- 25583377 | Background and objective: in this study, we evaluated survival in rheumatoid arthritis-associated pulmonary arterial hypertension (ra-pah) compared with idiopathic pulmonary arterial hypertension (ipah) patients, and evaluate differences in disease severity and treatment. |
| PubMedID- 21329286 | We sought to investigate observed vs expected mortality among geriatric ipah patients treated with specific pulmonary arterial hypertension (pah) therapy. |
| PubMedID- 22545094 | Phenotype labels: interstitial lung disease (ssc-ph-ild), idiopathic arterial hypertension (ipah), scleroderma with pulmonary arterial hypertension (ssc-pah), scleroderma (ssc), pulmonary arterial hypertension only (pah), idiopathic pulmonary fibrosis with pulmonary hypertension (ipf-ph), and human cord blood versus human adult blood (cbvab). |
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