Familial apoceruloplasmin deficiency Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C536004
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Genes

2 genes/proteins associated with the disease Familial apoceruloplasmin deficiency from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1 2.88009
CP ceruloplasmin (ferroxidase) 2.88009