RS786202403 SDHD
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hereditary cancer-predisposing syndrome
Cowden syndrome 3
Pheochromocytoma
Paragangliomas with sensorineural hearing loss
Carney-Stratakis syndrome
Hereditary pheochromocytoma and paraganglioma
Pheochromocytoma
Paragangliomas with sensorineural hearing loss
Cowden syndrome 3
Carney-Stratakis syndrome
Hereditary cancer-predisposing syndrome
Hereditary cancer-predisposing syndrome
Cowden syndrome 3
Pheochromocytoma
Paragangliomas with sensorineural hearing loss
Other Variants in SDHD