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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 3
1 OMIM reference -
7 associated genes
No signs/symptoms info
Rubinstein-Taybi syndrome due to CREBBP mutations
Acute promyelocytic leukemia

CREBBP NABP1
NPM1
NUMA1
PML
RARA
STAT5B
ZBTB16


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CREBBP
CREBBP
CREBBP
(0.9)
(0.63)
(0.63)
PML
RARA
STAT5B



Citations in the biomedical literature:


Rubinstein-Taybi syndrome due to CREBBP mutations
CREBBP
Acute promyelocytic leukemia
NABP1 NPM1 NUMA1 PML RARA STAT5B
ZBTB16



Rubinstein-Taybi syndrome due to CREBBP mutations
Acute promyelocytic leukemia

Synonym(s):
(no synonyms)

Synonym(s):
- Acute myeloblastic leukemia type 3
- Acute myeloid leukemia with t(15;17)(q22;q12);(PML/RARalpha) and variants

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):
- 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: D015473

No signs/symptoms info available.