EGLN1-related erythrocytosis and pheochromocytoma/paraganglioma predisposition

MONDO:1060184

Hereditary cancer predisposition due to variation(s) in the EGLN12 gene, which confers a predisposition to erythrocytosis and pheochromocytoma/paraganglioma.

Also known as: EGLN1-related erythrocytosis and pheochromocytoma/paraganglioma predisposition

32 clinical trials for this condition and its sub-types, 0 tagged with EGLN1-related erythrocytosis and pheochromocytoma/paraganglioma predisposition itself.

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↑ Hereditary neoplastic syndrome (731)

Including sub-types (32) Tagged with EGLN1-related erythrocytosis and pheochromocytoma/paraganglioma predisposition (0)

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