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Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
1 OMIM reference -
1 associated gene
No signs/symptoms info
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

NPHS1
(UniProt - OMIM)
 APP
(UniProt - OMIM)
PTPRO
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PTPRO
(0.56)
APP


Citations in the biomedical literature:


Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
NPHS1 PTPRO
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
(no synonyms)

Synonym(s):
- HCHWA, Flemish type
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Diseases of the genitourinary system -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.