Disease #02969 (COXPD4 (combined oxidative phosphorylation deficiency, type 4 (COXPD-4)), OMIM:610678)

Official abbreviation COXPD4
Name combined oxidative phosphorylation deficiency, type 4 (COXPD-4)
OMIM ID 610678
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 TUFM
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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00073552 - PubMed: Valente 2007 family, 1 affected, unaffected heterozygous carrier parents/sibs F no Italy Tyrol, south 01y02m - - - COXPD4 see paper; ..., died at 14m TUFM TUFM 1 1 Johan den Dunnen
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