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Hemoglobin Lepore - beta-thalassemia
2 associated genes
No signs/symptoms info
COMMON GENES: 1
Sickle cell - hemoglobin C disease
1 associated gene
No signs/symptoms info
Hemoglobin Lepore - beta-thalassemia
Sickle cell - hemoglobin C disease

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

COMMON
GENES 		HBB


Citations in the biomedical literature:


Hemoglobin Lepore - beta-thalassemia
HBB HBD
Sickle cell - hemoglobin C disease



Hemoglobin Lepore - beta-thalassemia
Sickle cell - hemoglobin C disease

Synonym(s):
- HbLepore - beta-thalassemia
- Lepore - beta-thalassemia
Synonym(s):
- HbSC disease
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: -
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.