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Hepatocellular carcinoma, childhood-onset
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
2 OMIM references -
3 associated genes
No signs/symptoms info
Hepatocellular carcinoma, childhood-onset
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes

CTNNB1
(UniProt - OMIM)
 NPHS1
(UniProt - OMIM)
MET
(UniProt - OMIM)
 NPHS2
(UniProt - OMIM)
PTPRO
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CTNNB1
MET
(0.68)
(0.68)
PTPRO
PTPRO


Citations in the biomedical literature:


Hepatocellular carcinoma, childhood-onset
CTNNB1 MET
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
NPHS1 NPHS2 PTPRO



Hepatocellular carcinoma, childhood-onset
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes

Classification (Orphanet):
- Rare hepatic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Diseases of the genitourinary system -
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.