Disease #05939 (MC1DN21 (mitochondrial complex I deficiency, nuclear type 21 (MC1DN21)), OMIM:618242)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MC1DN21
Name	mitochondrial complex I deficiency, nuclear type 21 (MC1DN21)
OMIM ID	618242
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	NUBPL
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-05-19 07:45:41 +02:00 (CEST)
Date last edited	N/A

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