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COMMON GENES: 2
PROTEIN INTERACTIONS: 2
1 OMIM reference -
3 associated genes
3 signs/symptoms
Hereditary persistence of fetal hemoglobin - sickle cell disease
Delta-beta-thalassemia

HBB HBB
HBG1 HBD
HBG2 HBG1
KLF1


COMMON
GENES
HBB
HBG1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
HBG2
HBG2
(0.52)
(0.49)
HBB
HBG1



Citations in the biomedical literature:


Hereditary persistence of fetal hemoglobin - sickle cell disease
HBB HBG1 HBG2 KLF1
Delta-beta-thalassemia
HBD



Hereditary persistence of fetal hemoglobin - sickle cell disease
Delta-beta-thalassemia

Synonym(s):
- HPFH - sickle cell disease

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

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

Delta-beta-thalassemia

Very frequent
- Anaemia
- Hemoglobinosis / hemoglobinopathy
- Microcytic anemia



Hereditary persistence of fetal hemoglobin - sickle cell disease

(no data available)