Searching map area
combined oxidative phosphorylation defect type 26
? TBD
human disease
Join to rate
Ratings 0
Nobody has rated this yet. Be the first!
Lists 0
Join to rate
Instance of
developmental defect during embryogenesis
Rare disease
class of disease
Subclass of
combined oxidative phosphorylation deficiency
autosomal recessive disease
References
Wikidata