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MIM:613559 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7
Echinobase Genes:
Human Disease Resource: MIM
DOID:0060286 - combined oxidative phosphorylation deficiency |
DOID:0111487 - combined oxidative phosphorylation deficiency 7 |
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DOID:0060286 - combined oxidative phosphorylation deficiency |
DOID:0111487 - combined oxidative phosphorylation deficiency 7 |