| 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 |
| Similar Terms | |
| Downloads & Tools |
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 |
