Disease #05041 (COXPD26 (oxidative phosphorylation deficiency, combined, type 26 (COXPD-26)), OMIM:616539)

Official abbreviation	COXPD26
Name	oxidative phosphorylation deficiency, combined, type 26 (COXPD-26)
OMIM ID	616539
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TRMT5
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 11:00:40 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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Global Variome shared LOVD