Hemochromatosis, type 3 Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Type 3 hemochromatosis 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_225123)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C537248
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Genes

1 genes/proteins associated with the disease Hemochromatosis, type 3 from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
TFR2 transferrin receptor 2 2.88009