Hemangiomatosis, familial pulmonary capillary: A rare condition involving the excessive proliferation of lung capillaries which results in pulmonary hypertension. More detailed information about the symptoms, causes, and treatments of Hemangiomatosis, familial pulmonary capillary is available below.
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Hemangiomatosis, familial pulmonary capillary is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Hemangiomatosis, familial pulmonary capillary, or a subtype of Hemangiomatosis, familial pulmonary capillary,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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