RS786205436 SDHD
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What This Variant Does
"CLNSIG=5
Associated Conditions
Fatal infantile mitochondrial cardiomyopathy
Mitochondrial complex 2 deficiency
nuclear type 3
Hereditary cancer-predisposing syndrome
Cowden syndrome 3
Carney-Stratakis syndrome
Paragangliomas with sensorineural hearing loss
Pheochromocytoma
Fatal infantile mitochondrial cardiomyopathy
Mitochondrial complex 2 deficiency
nuclear type 3
Hereditary cancer-predisposing syndrome
Cowden syndrome 3
Carney-Stratakis syndrome
Paragangliomas with sensorineural hearing loss
Other Variants in SDHD