Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6389
Gene Symbol: SDHA
SDHA
CUI: C0023264
Disease: Leigh Disease
Leigh Disease 		0.730 GeneticVariation UNIPROT Here, we characterize four patients with isolated complex II deficiency caused by mutations in SDHA presenting with multisystem mitochondrial disease including Leigh syndrome (LS) and/or leukodystrophy. 24781757

2015
Entrez Id: 6389
Gene Symbol: SDHA
SDHA
CUI: C0023264
Disease: Leigh Disease
Leigh Disease 		0.730 GeneticVariation UNIPROT Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndrome. 10746566

2000
Entrez Id: 6389
Gene Symbol: SDHA
SDHA
CUI: C0023264
Disease: Leigh Disease
Leigh Disease 		0.730 GeneticVariation UNIPROT Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency. 7550341

1995
Entrez Id: 6389
Gene Symbol: SDHA
SDHA
CUI: C3279992
Disease: PARAGANGLIOMAS 5
PARAGANGLIOMAS 5 		0.700 GeneticVariation UNIPROT SDHA is a tumor suppressor gene causing paraganglioma. 20484225

2010
Entrez Id: 6389
Gene Symbol: SDHA
SDHA
CUI: C1855008
Disease: Mitochondrial Complex II Deficiency
Mitochondrial Complex II Deficiency 		0.700 GeneticVariation UNIPROT

Entrez Id: 6389
Gene Symbol: SDHA
SDHA
CUI: C3150898
Disease: CARDIOMYOPATHY, DILATED, 1GG
CARDIOMYOPATHY, DILATED, 1GG 		0.600 GeneticVariation UNIPROT Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenase. 20551992

2010