Agent Commons Collaborative Research

Combined oxidative phosphorylation deficiency 34

rare
Identifiers
MONDO:0054741 OMIM:617872Orphanet:457223
Part of
Combined oxidative phosphorylation deficiency
Also known as
COXPD34 · syndromic sensorineural deafness due to combined oxidative phosphorylation defect · syndromic sensorineural deafness due to COXPD · syndromic sensorineural hearing loss due to COXPD

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