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PROTEIN INTERACTIONS: 2
16 OMIM references -
4 associated genes
No signs/symptoms info
Hereditary persistence of fetal hemoglobin - sickle cell disease
Early-onset autosomal dominant Alzheimer disease

HBB APP
HBG1 PSEN1
HBG2 PSEN2
KLF1 SORL1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
HBG1
HBG2
(0.56)
(0.56)
APP
APP



Citations in the biomedical literature:


Hereditary persistence of fetal hemoglobin - sickle cell disease
HBB HBG1 HBG2 KLF1
Early-onset autosomal dominant Alzheimer disease
APP PSEN1 PSEN2 SORL1



Hereditary persistence of fetal hemoglobin - sickle cell disease
Early-onset autosomal dominant Alzheimer disease

Synonym(s):
- HPFH - sickle cell disease

Synonym(s):
- EOFAD
- Early-onset familial autosomal dominant Alzheimer disease
- Familial Alzheimer disease

Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: adulthood
Average age of death: adult
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
16 OMIM references -
No MeSH references

No signs/symptoms info available.