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Diseases / Mitochondrial disease/ Inborn mitochondrial metabolism disorder/ Inborn mitochondrial myopathy

Mitochondrial complex II deficiency, nuclear type

rare

Identifiers: MONDO:0031230
Part of: Inborn mitochondrial myopathy

Subtypes

All diseases Rare only

Disease

Mitochondrial complex 2 deficiency, nuclear type 2 MONDO:0030935 SDHAF1
Mitochondrial complex 2 deficiency, nuclear type 3 MONDO:0030937 SDHD
Mitochondrial complex 2 deficiency, nuclear type 4 MONDO:0030974 SDHB
Mitochondrial complex II deficiency, nuclear type 1 MONDO:0100294 SDHA

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