| Dataset | DisGeNET 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 | https://www.disgenet.org/browser/0/1/0/C0521802 |
| Similar Terms | |
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2 genes associated with the disease Congenital Atransferrinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
