Statements (30)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:genetic_disorder
gptkb:blood_disorder |
| gptkbp:affects |
gptkb:hemoglobin
|
| gptkbp:causedBy |
mutation in HBA1 gene
mutation in HBA2 gene |
| gptkbp:diagnosedBy |
gptkb:blood_test
genetic testing |
| gptkbp:firstDescribed |
1960s
|
| gptkbp:ICD-10_code |
D56.0
|
| gptkbp:inheritsFrom |
autosomal recessive
|
| gptkbp:MeSH_ID |
D013789
|
| gptkbp:OMIM |
604131
|
| gptkbp:prevalence |
gptkb:Africa
gptkb:Southeast_Asia gptkb:Mediterranean_region |
| gptkbp:subspecies |
Hydrops fetalis
Alpha-thalassemia trait Hemoglobin H disease Silent carrier |
| gptkbp:symptom |
gptkb:anemia
fatigue jaundice enlarged spleen pale skin |
| gptkbp:treatment |
blood transfusion
bone marrow transplant folic acid supplements |
| gptkbp:bfsParent |
gptkb:chromosome_16p13.3
|
| gptkbp:bfsLayer |
8
|
| http://www.w3.org/2000/01/rdf-schema#label |
Alpha-thalassemia
|