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combined oxidative phosphorylation deficiency
?
TBD
Human disease
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Subclasses
7
Influences rating
pontocerebellar hypoplasia type 6
human disease
combined oxidative phosphorylation defect type 26
human disease
combined oxidative phosphorylation defect type 27
human disease
leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome
human disease
neonatal severe cardiopulmonary failure due to mitochondrial methylation defect
human disease
combined oxidative phosphorylation defect type 25
human disease
combined oxidative phosphorylation defect type 30
human disease
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Instance of
Rare disease
developmental defect during embryogenesis
class of disease
Subclass of
Mitochondrial disease
Wikidata
