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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 2
1 OMIM reference -
2 associated genes
No signs/symptoms info
Rubinstein-Taybi syndrome due to CREBBP mutations
Myelodysplastic syndromes

CREBBP GATA2
MECOM


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CREBBP
CREBBP
(0.87)
(0.56)
MECOM
GATA2



Citations in the biomedical literature:


Rubinstein-Taybi syndrome due to CREBBP mutations
CREBBP
Myelodysplastic syndromes
GATA2 MECOM



Rubinstein-Taybi syndrome due to CREBBP mutations
Myelodysplastic syndromes

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):
(no data available)

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D009190

No signs/symptoms info available.