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1 OMIM reference -
3 associated genes
3 signs/symptoms
COMMON GENES: 1
COMMON SIGNS: 2
1 associated gene
4 signs/symptoms
Delta-beta-thalassemia
Hemoglobin E - beta-thalassemia

HBB HBB
HBD
HBG1


COMMON
GENES
HBB



Citations in the biomedical literature:


Delta-beta-thalassemia
HBB HBD HBG1
Hemoglobin E - beta-thalassemia



Delta-beta-thalassemia
Hemoglobin E - beta-thalassemia

Synonym(s):
(no synonyms)

Synonym(s):
- E-beta-thalassemia
- HbE - beta-thalassemia

Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease

Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive

External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references


COMMON
SIGNS
- Anaemia
- Hemoglobinosis / hemoglobinopathy


Delta-beta-thalassemia
Hemoglobin E - beta-thalassemia

Very frequent
- Microcytic anemia



Very frequent
- Immunodeficiency / increased susceptibility to infections / recurrent infections

Frequent
- Hyperferritinemia / iron overload