C190373Level 6
Hereditary Paraganglioma-Pheochromocytoma Syndrome
**Semantic type:** Disease or Syndrome
**Definition:** A hereditary cancer syndrome characterized by the development of multiple paragangliomas including pheochromocytomas. It is caused by mutations in SDHA, SDHB, SDHC, SDHD, and SDHAF2 genes.
**Synonyms:** - Familial Paraganglioma-Pheochromocytoma Syndrome - Familial Pheochromocytoma-Paraganglioma Syndrome - Hereditary Pheochromocytoma-Paraganglioma Syndrome
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