Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
genetic disorder
hemoglobin |
| gptkbp:affects |
hemoglobin production
|
| gptkbp:alsoKnownAs |
beta-thalassemia trait
|
| gptkbp:causedBy |
mutation in HBB gene
|
| gptkbp:diagnosedBy |
complete blood count
hemoglobin electrophoresis |
| gptkbp:differentialDiagnosis |
iron deficiency anemia
|
| https://www.w3.org/2000/01/rdf-schema#label |
beta-thalassemia minor
|
| gptkbp:ICD-10_code |
gptkb:D56.3
|
| gptkbp:inheritance |
autosomal recessive
|
| gptkbp:inheritanceRisk |
25% chance of major if both parents have minor
|
| gptkbp:OMIM |
141900
|
| gptkbp:prevalence |
high in Mediterranean populations
high in Middle Eastern populations high in South Asian populations |
| gptkbp:riskFactor |
offspring may inherit beta-thalassemia major if both parents are carriers
|
| gptkbp:symptom |
microcytosis
hypochromia mild anemia |
| gptkbp:treatment |
usually not required
|
| gptkbp:bfsParent |
gptkb:beta-thalassemia
|
| gptkbp:bfsLayer |
6
|