Disease #04496 (COXPD23 (oxidative phosphorylation deficiency, combined, type 23 (COXPD-23)), OMIM:616198)

Official abbreviation COXPD23
Name oxidative phosphorylation deficiency, combined, type 23 (COXPD-23)
OMIM ID 616198
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene GTPBP3
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00305941 40 - - F - China - - - - - COXPD23 - GTPBP3 GTPBP3 2 1 Sha Hong
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