Disease #05060 (COXPD20 (oxidative phosphorylation deficiency, combined, type 20 (COXPD-20)), OMIM:615917)

Official abbreviation	COXPD20
Name	oxidative phosphorylation deficiency, combined, type 20 (COXPD-20)
OMIM ID	615917
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	VARS2
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