Disease #00575

Official abbreviation	301020
Name	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 12; MC1DN12
OMIM ID	301020
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	NDUFA1
Associated tissues	-
Disease features	-
Remarks	-