Disease #03362 (COXPD7 (combined oxidative phosphorylation deficiency, type 7 (COXPD-7)), OMIM:613559)

Official abbreviation COXPD7
Name combined oxidative phosphorylation deficiency, type 7 (COXPD-7)
OMIM ID 613559
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 C12orf65
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00080916 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - COXPD7 Combined oxidative phosphorylation deficiency 7 (OMIM:613559) C12orf65 C12orf65 1 1 Daniel Trujillano
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