Dursun syndrome

MONDO:0023124

A syndromic disease caused by mutation in the G6PC3 gene, characterized by familial pulmonary arterial hypertension, leukopenia, and atrial septal defect.

Also known as: familial pulmonary arterial hypertension leucopenia and atrial septal defect, familial pulmonary arterial hypertension, leucopenia, and atrial septal defect, familial PAH, leucopenia and ASD, familial pulmonary arterial hypertension, leucopenia and ASD

0 clinical trials for this condition and its sub-types, 0 tagged with Dursun syndrome itself.

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↑ Hereditary disease (18187) ↑ Syndromic disease (7133)

Including sub-types (0) Tagged with Dursun syndrome (0)

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