combined oxidative phosphorylation deficiency 29
human disease
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Summary
combined oxidative phosphorylation deficiency 29 is a developmental defect during embryogenesis[1]. It is known by 3 alternative names across languages and contexts.[2]
Key Facts
- combined oxidative phosphorylation deficiency 29's instance of is recorded as developmental defect during embryogenesis[3].
- combined oxidative phosphorylation deficiency 29's instance of is recorded as rare disease[4].
- combined oxidative phosphorylation deficiency 29's instance of is recorded as class of disease[5].
- combined oxidative phosphorylation deficiency 29 is a type of autosomal recessive disease[6].
- combined oxidative phosphorylation deficiency 29 is a type of combined oxidative phosphorylation deficiency[7].
- combined oxidative phosphorylation deficiency 29's genetic association is recorded as TXN2[8].
- combined oxidative phosphorylation deficiency 29's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111501[9].
- combined oxidative phosphorylation deficiency 29's exact match is recorded as http://identifiers.org/doid/DOID:0111501[10].
Why It Matters
combined oxidative phosphorylation deficiency 29 is known by 3 alternative names across languages and contexts.[2]