Disease #05955 (MC4DN1 (mitochondrial complex IV deficiency, nuclear, type 1 (MC4DN1)), OMIM:220110)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MC4DN1
Name	mitochondrial complex IV deficiency, nuclear, type 1 (MC4DN1)
OMIM ID	220110
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive, Mitochondrial
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SURF1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-07-23 10:41:14 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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