Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4536
Gene Symbol: ND2
ND2
CUI: C1838979
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY
MITOCHONDRIAL COMPLEX I DEFICIENCY 		0.400 GermlineCausalMutation ORPHANET Nonsense mutations in mitochondrial DNA associated with myalgia and exercise intolerance. 15781840

2005
Entrez Id: 4536
Gene Symbol: ND2
ND2
CUI: C1838979
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY
MITOCHONDRIAL COMPLEX I DEFICIENCY 		0.400 GermlineCausalMutation ORPHANET Paternal inheritance of mitochondrial DNA. 12192017

2002