Hemochromatosis, type 4 Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Hemochromatosis type 4 (also called ferroportin disease) is a form of rare hereditary hemochromatosis (HH; see this term), a group of diseases characterized by excessive tissue iron deposition of genetic origin. (Orphanet Rare Disease Ontology, Orphanet_139491)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C537249
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Genes

1 genes/proteins associated with the disease Hemochromatosis, type 4 from the curated CTD Gene-Disease Associations dataset.

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