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2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
Familial rhabdoid tumor
Hereditary persistence of fetal hemoglobin - sickle cell disease

SMARCA4 HBB
SMARCB1 HBG1
HBG2
KLF1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
SMARCB1
SMARCA4
(0.85)
(0.75)
KLF1
KLF1



Citations in the biomedical literature:


Familial rhabdoid tumor
SMARCA4 SMARCB1
Hereditary persistence of fetal hemoglobin - sickle cell disease
HBB HBG1 HBG2 KLF1



Familial rhabdoid tumor
Hereditary persistence of fetal hemoglobin - sickle cell disease

Synonym(s):
- RTPS
- Rhabdoid tumor predisposition syndrome

Synonym(s):
- HPFH - sickle cell disease

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

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

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal recessive

External references:
2 OMIM references -
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.