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Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
2 OMIM references -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Craniopharyngioma
2 associated genes
No signs/symptoms info
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
Craniopharyngioma

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

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


Citations in the biomedical literature:


Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
NPHS1 NPHS2 PTPRO
Craniopharyngioma
BRAF CTNNB1



Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
Craniopharyngioma

Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare endocrine disease
- Rare neurologic disease
- Rare oncologic disease
Classification (ICD10):
- Diseases of the genitourinary system -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: variable
Average age of death: -
Type of inheritance: sporadic
External references:
2 OMIM references -
No MeSH references
External references:
No OMIM references
1 MeSH reference: D003397
No signs/symptoms info available.