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Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
1 associated gene
No signs/symptoms info
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis

CREBBP
(UniProt - OMIM)
 WT1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CREBBP
(0.65)
WT1


Citations in the biomedical literature:


Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
CREBBP
Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
WT1



Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis

Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare endocrine disease
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
- Rare oncologic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the genitourinary system -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.