PedAM
Pediatric Disease Annotations & Medicines
| Disease | pulmonary hypertension |
| Phenotype | C0039445|hereditary haemorrhagic telangiectasia |
| Sentences | 3 |
| PubMedID- 23919827 | Background: mutations in activin receptor-like kinase-1 (acvrl-1) or endoglin (eng) are mostly identified in patients with hereditary haemorrhagic telangiectasia (hht) associated with pulmonary hypertension (ph), but have not yet been studied in chinese patients. |
| PubMedID- 26015855 | pulmonary hypertension in hereditary haemorrhagic telangiectasia. |
| PubMedID- 23378554 | pulmonary hypertension in a patient with hereditary haemorrhagic telangiectasia. |
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