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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
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
1 OMIM reference -
1 associated gene
No signs/symptoms info
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia

NPHS1
(UniProt - OMIM)
 CBL
(UniProt - OMIM)
NPHS2
(UniProt - OMIM)
PTPRO
(UniProt - OMIM)

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


Citations in the biomedical literature:


Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
NPHS1 NPHS2 PTPRO
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
CBL



Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia

Synonym(s):
(no synonyms)

Synonym(s):
- CBL syndrome
- Noonan syndrome-like disorder with JMML
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare cardiac disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare oncologic disease
Classification (ICD10):
- Diseases of the genitourinary system -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
2 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.