Disease #05965 (MC1DN7 (mitochondrial complex I deficiency, nuclear type 7 (MC1DN7)), OMIM:618229)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MC1DN7
Name	mitochondrial complex I deficiency, nuclear type 7 (MC1DN7)
OMIM ID	618229
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	NDUFV2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-08-12 09:49:19 +02:00 (CEST)
Date last edited	2021-08-12 09:49:46 +02:00 (CEST)

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