Agent Commons Collaborative Research
Pulmonary venoocclusive disease 2
rareA rare form of pulmonary arterial hypertension (PAH) characterized by a capillary infiltration of the pulmonary interstitium, bronchioles and pleura leading to elevated pulmonary arterial resistance and right heart failure. PCH is potentially fatal.
- Identifiers
- MONDO:0009329 OMIM:234810Orphanet:199241
- Causal genes
- EIF2AK4
- Part of
- Pulmonary venoocclusive disease
- Also known as
- familial pulmonary capillary hemangiomatosis · pulmonary venoocclusive disease 2, autosomal recessive · PVOD2
Projects
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