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COMMON GENES: 1
PROTEIN INTERACTIONS: 5
3 associated genes
No signs/symptoms info
Hereditary persistence of fetal hemoglobin - sickle cell disease
Autosomal dominant methemoglobinemia

HBB HBA1
HBG1 HBA2
HBG2 HBB
KLF1


COMMON
GENES
HBB


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
HBB
HBB
HBG2
HBG2
HBG2
(0.96)
(0.96)
(0.72)
(0.72)
(0.52)
HBA1
HBA2
HBA1
HBA2
HBB



Citations in the biomedical literature:


Hereditary persistence of fetal hemoglobin - sickle cell disease
HBB HBG1 HBG2 KLF1
Autosomal dominant methemoglobinemia
HBA1 HBA2



Hereditary persistence of fetal hemoglobin - sickle cell disease
Autosomal dominant methemoglobinemia

Synonym(s):
- HPFH - sickle cell disease

Synonym(s):
- Hemoglobin M disease
- Hereditary methemoglobinemia due to hemoglobin mutation
- M hemoglobinopathy

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: -
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.