Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1356
Gene Symbol: CP
CP
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.130 GeneticVariation CLINVAR Aceruloplasminaemia: a family with a novel mutation and long-term therapy with deferasirox. 25089372

2015
Entrez Id: 1356
Gene Symbol: CP
CP
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.130 GeneticVariation CLINVAR Aceruloplasminemia: a novel mutation in a family with marked phenotypic variability. 18200628

2008
Entrez Id: 1356
Gene Symbol: CP
CP
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.130 GeneticVariation CLINVAR Molecular and pathological basis of aceruloplasminemia. 16629161

2006
Entrez Id: 1356
Gene Symbol: CP
CP
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.130 GeneticVariation CLINVAR Aceruloplasminemia, an iron metabolic disorder. 14719552

2003