CP, ceruloplasmin, 1356

N. diseases: 283; N. variants: 64
Disease: Movement Disorders ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs750451693
rs750451693
Entrez Id: 1356
Gene Symbol: CP
CP
CUI: C0026650
Disease:
Movement Disorders 		T 0.700 GeneticVariation CLINVAR Aceruloplasminaemia: a family with a novel mutation and long-term therapy with deferasirox. 25089372 2015
dbSNP: rs750451693
rs750451693
Entrez Id: 1356
Gene Symbol: CP
CP
CUI: C0026650
Disease:
Movement Disorders 		T 0.700 GeneticVariation CLINVAR Aceruloplasminemia: a novel mutation in a family with marked phenotypic variability. 18200628 2008
dbSNP: rs750451693
rs750451693
Entrez Id: 1356
Gene Symbol: CP
CP
CUI: C0026650
Disease:
Movement Disorders 		T 0.700 GeneticVariation CLINVAR Molecular and pathological basis of aceruloplasminemia. 16629161 2006
dbSNP: rs750451693
rs750451693
Entrez Id: 1356
Gene Symbol: CP
CP
CUI: C0026650
Disease:
Movement Disorders 		T 0.700 GeneticVariation CLINVAR Aceruloplasminemia, an iron metabolic disorder. 14719552 2003