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Summary Literature (0)
MIM:601650 - PHEOCHROMOCYTOMA/PARAGANGLIOMA SYNDROME 2; PPGL2

Xenbase Genes: sdhaf2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011121 - pheochromocytoma/paraganglioma syndrome 2
MONDO:0017366 - hereditary pheochromocytoma-paraganglioma

Disease Ontology (DO):
DOID:0050773 - paraganglioma