CP, ceruloplasmin, 1356

N. diseases: 283; N. variants: 64
Disease: Involuntary Movements ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0427086
Disease: Involuntary Movements
Involuntary Movements 		0.310 Biomarker phenotype CTD_human Aceruloplasminemia, an inherited disorder of iron metabolism. 12572680 2003
CUI: C0427086
Disease: Involuntary Movements
Involuntary Movements 		0.310 Biomarker phenotype BEFREE Three sporadic patients (two men and one woman) were examined with involuntary movements and dysarthria associated with abnormal concentrations of serum copper, serum ceruloplasmin, and urinary copper excretion. 11723201 2001