Congenital atransferrinemia Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Congenital atransferrinemia is a very rare hematologic disease caused by a transferrin (TF) deficiency and characterized by microcytic, hypochromic anemia (manifesting with pallor, fatigue and growth retardation) and iron overload, and that can be fatal if left untreated. (Orphanet Rare Disease Ontology, Orphanet_1195)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C538259
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Genes

1 genes/proteins associated with the disease Congenital atransferrinemia from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
TF transferrin 2.88009