Disease #00576

MSeqDR-LSDB Mitochondrial Disease Locus Specific Database

LOVD v.3.0 Build 21 [ Current LOVD status ]
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	Curator: Lishuang Shen

Official abbreviation	301021
Name	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 30; MC1DN30
OMIM ID	301021
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	NDUFB11
Associated tissues	-
Disease features	-
Remarks	-