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PROTEIN INTERACTIONS: 1
3 OMIM references -
3 associated genes
No signs/symptoms info
Hereditary persistence of fetal hemoglobin - sickle cell disease
Neurofibromatosis type 3

HBB LZTR1
HBG1 NF2
HBG2 SMARCB1
KLF1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
KLF1
(0.85)
SMARCB1



Citations in the biomedical literature:


Hereditary persistence of fetal hemoglobin - sickle cell disease
HBB HBG1 HBG2 KLF1
Neurofibromatosis type 3
LZTR1 NF2 SMARCB1



Hereditary persistence of fetal hemoglobin - sickle cell disease
Neurofibromatosis type 3

Synonym(s):
- HPFH - sickle cell disease

Synonym(s):
- NF3
- Neurilemmomatosis
- Schwannomatosis

Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
- Rare oncologic disease
- Rare skin disease

Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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

External references:
No OMIM references
No MeSH references
External references:
3 OMIM references -
1 MeSH reference: C536641

No signs/symptoms info available.