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PROTEIN INTERACTIONS: 1
2 associated genes
No signs/symptoms info
Hereditary persistence of fetal hemoglobin - sickle cell disease
Peripheral primitive neuroectodermal tumor

HBB ERG
HBG1 FLI1
HBG2
KLF1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
KLF1
(0.79)
FLI1



Citations in the biomedical literature:


Hereditary persistence of fetal hemoglobin - sickle cell disease
HBB HBG1 HBG2 KLF1
Peripheral primitive neuroectodermal tumor
ERG FLI1



Hereditary persistence of fetal hemoglobin - sickle cell disease
Peripheral primitive neuroectodermal tumor

Synonym(s):
- HPFH - sickle cell disease

Synonym(s):
- PPNET
- Peripheral PNET

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

Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)

External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.