Disease #04419 (MC4DN9;CEMCOX3 (mitochondrial complex IV deficiency, type 9 (MC4DN9, CEMCOX3)), OMIM:616500)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MC4DN9;CEMCOX3
Name	mitochondrial complex IV deficiency, type 9 (MC4DN9, CEMCOX3)
OMIM ID	616500
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	COA5
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:22 +02:00 (CEST)
Date last edited	2021-10-18 19:54:38 +02:00 (CEST)

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