RS80338844 SDHD
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What This Variant Does
"[OMIM:?]
Associated Conditions
Pheochromocytoma
Pheochromocytoma/paraganglioma syndrome 1
Hereditary pheochromocytoma and paraganglioma
Hereditary cancer-predisposing syndrome
Carney-Stratakis syndrome
Mitochondrial complex II deficiency
nuclear type 1
Paragangliomas with sensorineural hearing loss
Cowden syndrome 3
Mitochondrial complex 2 deficiency
nuclear type 3
SDHD-related disorder
Inherited phaeochromocytoma and paraganglioma excluding NF1
Paraganglioma
Paragangliomas with sensorineural hearing loss
Other Variants in SDHD