CYCS, cytochrome c, somatic, 54205

N. diseases: 67; N. variants: 4
Disease: Hyperferritinemia, hereditary, with congenital cataracts ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1833213
Disease: Hyperferritinemia, hereditary, with congenital cataracts
Hyperferritinemia, hereditary, with congenital cataracts 		0.010 AlteredExpression disease BEFREE Taken together, spontaneous mutation in the IRE of L-ferritin may cause non-H-HCS by the same mechanism as HHCS. 19800271 2010