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1 OMIM reference -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
2 associated genes
No signs/symptoms info
Alveolar rhabdomyosarcoma
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis

FOXO1 PKD1
PAX3 TSC2
PAX7


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
FOXO1
(0.79)
TSC2



Citations in the biomedical literature:


Alveolar rhabdomyosarcoma
FOXO1 PAX3 PAX7
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
PKD1 TSC2



Alveolar rhabdomyosarcoma
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis

Synonym(s):
(no synonyms)

Synonym(s):
- Tuberous sclerosis/polycystic kidney disease contiguous gene syndrome

Classification (Orphanet):
- Rare oncologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare renal disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
(no data available)

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: D018232
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.