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Sickle cell - hemoglobin E disease
1 associated gene
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 1
Hereditary persistence of fetal hemoglobin - sickle cell disease
4 associated genes
No signs/symptoms info
Sickle cell - hemoglobin E disease
Hereditary persistence of fetal hemoglobin - sickle cell disease

HBB
(UniProt - OMIM)
 HBB
(UniProt - OMIM)
HBG1
(UniProt - OMIM)
HBG2
(UniProt - OMIM)
KLF1
(UniProt - OMIM)

COMMON
GENES 		HBB
INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
HBB
(0.52)
HBG2


Citations in the biomedical literature:


Sickle cell - hemoglobin E disease
HBB
Hereditary persistence of fetal hemoglobin - sickle cell disease
HBG1 HBG2 KLF1



Sickle cell - hemoglobin E disease
Hereditary persistence of fetal hemoglobin - sickle cell disease

Synonym(s):
- HbSE disease
Synonym(s):
- HPFH - sickle cell 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: variable
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.