CYTB, cytochrome b, 4519

N. diseases: 166; N. variants: 83
Disease: Histiocytoid Cardiomyopathy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1708371
Disease: Histiocytoid Cardiomyopathy
Histiocytoid Cardiomyopathy 		0.510 GeneticVariation disease BEFREE A missense mutation in the mitochondrial cytochrome b gene in a revisited case with histiocytoid cardiomyopathy. 10960495 2000
CUI: C1708371
Disease: Histiocytoid Cardiomyopathy
Histiocytoid Cardiomyopathy 		0.510 GeneticVariation disease ORPHANET A missense mutation in the mitochondrial cytochrome b gene in a revisited case with histiocytoid cardiomyopathy. 10960495 2000
CUI: C1708371
Disease: Histiocytoid Cardiomyopathy
Histiocytoid Cardiomyopathy 		0.510 GeneticVariation disease UNIPROT A missense mutation in the mitochondrial cytochrome b gene in a revisited case with histiocytoid cardiomyopathy. 10960495 2000