CYTB, cytochrome b, 4519

N. diseases: 166; N. variants: 83
Disease: Mitochondrial Encephalomyopathies ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0162666
Disease: Mitochondrial Encephalomyopathies
Mitochondrial Encephalomyopathies 		0.110 GeneticVariation disease BEFREE Mitochondrial encephalomyopathy and complex III deficiency associated with a stop-codon mutation in the cytochrome b gene. 11047755 2000
CUI: C0162666
Disease: Mitochondrial Encephalomyopathies
Mitochondrial Encephalomyopathies 		0.110 CausalMutation disease CLINVAR