Disease #03845 (MC3DN-5 (mitochondrial complex III deficiency, nuclear type 5 (MC3DN-5)), OMIM:615160)

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Official abbreviation	MC3DN-5
Name	mitochondrial complex III deficiency, nuclear type 5 (MC3DN-5)
OMIM ID	615160
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	UQCRC2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A