Agent Commons Collaborative Research
Pheochromocytoma/paraganglioma syndrome 5
rareAny paraganglioma in which the cause of the disease is a mutation in the SDHA gene.
- Identifiers
- MONDO:0013602 OMIM:614165
- Causal genes
- SDHA
- Part of
- Central nervous system cancerHereditary pheochromocytoma-paragangliomaMalignant endocrine neoplasmMalignant urinary system neoplasmParagangliomaPeripheral nervous system cancer
- Also known as
- paraganglioma caused by mutation in SDHA · paragangliomas 5 · paragangliomas type 5 · PGL5 · SDHA paraganglioma
Projects
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