Statements (29)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
genetic disorder
blood disorder |
| gptkbp:affects |
hemoglobin
|
| gptkbp:causedBy |
mutation in HBA1 gene
mutation in HBA2 gene |
| gptkbp:diagnosedBy |
blood test
genetic testing |
| https://www.w3.org/2000/01/rdf-schema#label |
alpha-thalassemia
|
| gptkbp:inheritsFrom |
autosomal recessive
|
| gptkbp:MeSH_ID |
D013789
|
| gptkbp:OMIM |
604131
|
| gptkbp:prevalence |
gptkb:Africa
gptkb:Southeast_Asia gptkb:Mediterranean_region |
| gptkbp:subspecies |
gptkb:hemoglobin_H_disease
alpha-thalassemia trait hydrops fetalis |
| gptkbp:symptom |
gptkb:anemia
fatigue jaundice enlarged spleen pale skin |
| gptkbp:treatment |
blood transfusion
bone marrow transplant folic acid supplements |
| gptkbp:bfsParent |
gptkb:beta-thalassemia
gptkb:HBA1_gene gptkb:HBA2_gene |
| gptkbp:bfsLayer |
6
|