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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Rubinstein-Taybi syndrome due to CREBBP mutations
Myeloid neoplasm associated with FGFR1 rearrangement

CREBBP FGFR1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CREBBP
(0.67)
FGFR1



Citations in the biomedical literature:


Rubinstein-Taybi syndrome due to CREBBP mutations
CREBBP
Myeloid neoplasm associated with FGFR1 rearrangement
FGFR1



Rubinstein-Taybi syndrome due to CREBBP mutations
Myeloid neoplasm associated with FGFR1 rearrangement

Synonym(s):
(no synonyms)

Synonym(s):
- 8p11 myeloproliferative syndrome
- Stem cell leukemia/lymphoma

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 hematologic disease
- Rare oncologic disease

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