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: rs1553759167
rs1553759167
Entrez Id: 1356
Gene Symbol: CP
CP
CUI: C0878682
Disease:
Ceruloplasmin deficiency 		G 0.700 CausalMutation CLINVAR Movement disorders and brain iron overload in a new subtype of aceruloplasminemia. 25864092 2015