Human disease · combined oxidative phosphorylation deficiency · YYNN

combined oxidative phosphorylation deficiency

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Human disease

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Subclasses
7

pontocerebellar hypoplasia type 6

combined oxidative phosphorylation defect type 26

combined oxidative phosphorylation defect type 27

leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome

neonatal severe cardiopulmonary failure due to mitochondrial methylation defect

combined oxidative phosphorylation defect type 25

combined oxidative phosphorylation defect type 30

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Instance of

developmental defect during embryogenesis

class of disease

Subclass of

Mitochondrial disease

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