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Pulmonary arterial hypertension associated with schistosomiasis

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Disease definition

Pulmonary arterial hypertension associated with schistosomiasis (PAHS) is a form of pulmonary arterial hypertension characterized by an elevated pulmonary arterial resistance leading to right heart failure, observed as a complication of a chronic schistosomiasis.

ORPHA:275823

Classification level: Group of disorders

Synonym(s):
  • PAH associated with schistosomiasis

Prevalence: Unknown

Inheritance: Not applicable

Age of onset: All ages

UMLS: C3697477

A summary on this disease is available in Español, Nederlands
Detailed information

Logo ERN: produced/endorsed by ERN(s) Logo FSMR: produced/endorsed by FSMR(s)

General public
Guidelines
Emergency guidelines
Français (2020.pdf) - Orphanet Urgences
Clinical practice guidelines
English (2016) - Eur Heart J Logo ERN
English (2023) - Eur J Heart Fail Logo ERN
English (2022) - Eur Heart J Logo ERN
English (2011) - Int J Cardiol Logo ERN
Disease review articles
Review article
English (2013) - Orphanet J Rare Dis
Patient-Centered Outcome Measures (PCOMs)
Access questionnaires assessing quality of life in this disease (English)
The documents contained in this website are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.