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Summary Literature (0)
MIM:171300 - PHEOCHROMOCYTOMA

Xenbase Genes: gdnf, ret, vhl, sdhb, kif1b, sdhd, tmem127, max

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008233 - pheochromocytoma
MONDO:0017366 - hereditary pheochromocytoma-paraganglioma

Disease Ontology (DO):
DOID:0050771 - pheochromocytoma