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loading...| Preferred Name |
Delta-beta-thalassemia |
| ID |
http://www.orpha.net/ORDO/Orphanet_231237 |
| definition |
Delta-beta-thalassemia is a form of beta-thalassemia (see this term) characterized by decreased or absent synthesis of the delta- and beta-globin chains with a compensatory increase in expression of fetal gamma-chain synthesis. |
| definition_citation |
Orphanet |
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=231237 |
| has_age_of_onset |
Neonatal Infancy |
| has_inheritance |
Autosomal recessive |
| hasDbXref |
OMIM:141749 ICD-10:D56.2 ICD-11:3A50.3 MedDRA:10012236 UMLS:C0271985 |
| label |
Delta-beta-thalassemia |
| notation |
ORPHA:231237 |
| part_of | |
| prefixIRI |
ORDO:Orphanet_231237 |
| prefLabel |
Delta-beta-thalassemia |
| present_in |
Worldwide AND has_point_prevalence_range : Unknown |
| treeView | |
| subClassOf |
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