Disease #05956 (MC4DN20 (mitochondrial complex IV deficiency, nuclear, type 20 (MC4DN20)), OMIM:619064)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MC4DN20
Name	mitochondrial complex IV deficiency, nuclear, type 20 (MC4DN20)
OMIM ID	619064
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	COX5A
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-07-23 10:42:56 +02:00 (CEST)
Date last edited	N/A

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