CP, ceruloplasmin, 1356

N. diseases: 283; N. variants: 64
Disease: Ceruloplasmin deficiency ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs386134133
rs386134133
Entrez Id: 1356
Gene Symbol: CP
CP
CUI: C0878682
Disease:
Ceruloplasmin deficiency 		T 0.700 CausalMutation CLINVAR Hepatic iron overload associated with a decreased serum ceruloplasmin level in a novel clinical type of aceruloplasminemia. 16831606 2006