hereditary pheochromocytoma-paraganglioma
ORPHA: 29072
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with hereditary pheochromocytoma-paraganglioma, sourced from HPO and Orphanet clinical annotations.
ParagangliomaExtraadrenal pheochromocytomaAdrenal pheochromocytomaProteinuriaGlomerular sclerosisEpisodic paroxysmal anxietyEpisodic hyperhidrosisHypertensive retinopathyCerebral hemorrhageDysphoniaWeight lossPalpitationsNauseaRecurrent paroxysmal headacheEpisodic abdominal painHypertension associated with pheochromocytomaParaganglioma of head and neckHypercalcemiaElevated urinary norepinephrine levelPositive regitine blocking testElevated urinary epinephrine levelPulsatile tinnitusParoxysmal vertigoSinus tachycardiaElevated urinary dopamine levelFatigueFlushingChest painConductive hearing impairmentHematuriaPallorCranial nerve compressionTremorVocal cord paralysisCongestive heart failureElevated circulating calcitonin concentrationRenal cell carcinomaRetinal capillary hemangiomaArachnoid hemangiomatosisPanic attackAniridia
Classification & Codes
Orphanet Code
ORPHA:29072hereditary pheochromocytoma-paraganglioma
| Orphanet | ORPHA:29072 |
| Treatments | 0 drug(s) |
| Symptoms on record | 41 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO