CYTB, cytochrome b, 4519

N. diseases: 166; N. variants: 83
Disease: MELAS Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0162671
Disease: MELAS Syndrome
MELAS Syndrome 		0.310 GeneticVariation disease BEFREE A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndrome. 9894888 1999
CUI: C0162671
Disease: MELAS Syndrome
MELAS Syndrome 		0.310 Biomarker disease CTD_human