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Hemoglobin C - beta-thalassemia
1 associated gene
4 signs/symptoms
COMMON GENES: 1
Hemoglobin E disease
1 associated gene
No signs/symptoms info
Hemoglobin C - beta-thalassemia
Hemoglobin E disease

HBB
(UniProt - OMIM)
 HBB
(UniProt - OMIM)

COMMON
GENES 		HBB


Citations in the biomedical literature:


Hemoglobin C - beta-thalassemia
HBB
Hemoglobin E disease



Hemoglobin C - beta-thalassemia
Hemoglobin E disease

Synonym(s):
- C- beta-thalassemia
- HbC - beta-thalassemia
Synonym(s):
(no synonyms)
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: -
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: any age
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
Hemoglobin C - beta-thalassemia

Very frequent
- Anaemia
- Hemoglobinosis / hemoglobinopathy
- Microcytic anemia
- Splenomegaly



Hemoglobin E disease

(no data available)