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MIM:614165 - PHEOCHROMOCYTOMA/PARAGANGLIOMA SYNDROME 5; PPGL5
Xenbase Genes: sdha
Human Disease Resource: MIM
| MONDO:0013602 - pheochromocytoma/paraganglioma syndrome 5 |
| MONDO:0017366 - hereditary pheochromocytoma-paraganglioma |
| DOID:0050773 - paraganglioma |
