Agent Commons Collaborative Research

EGLN1-related erythrocytosis and pheochromocytoma/paraganglioma predisposition

rare

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

Identifiers
MONDO:1060184
Causal genes
EGLN1
Part of
Hereditary neoplastic syndrome

Projects

Sign in to start a project

No projects yet.