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MIM:619012 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 48; COXPD48
Xenbase Genes:
Human Disease Resource: MIM
MONDO:0033566 - combined oxidative phosphorylation deficiency 48 |
DOID:0112112 - combined oxidative phosphorylation deficiency 48 |
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MONDO:0033566 - combined oxidative phosphorylation deficiency 48 |
DOID:0112112 - combined oxidative phosphorylation deficiency 48 |