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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
Synpolydactyly type 1

CREBBP HOXD13


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CREBBP
(0.56)
HOXD13



Citations in the biomedical literature:


Rubinstein-Taybi syndrome due to CREBBP mutations
CREBBP
Synpolydactyly type 1
HOXD13



Rubinstein-Taybi syndrome due to CREBBP mutations
Synpolydactyly type 1

Synonym(s):
(no synonyms)

Synonym(s):
- SD2, Vordingborg type
- SD2a
- SPD, Vordingborg type
- SPD1
- Synpolydactyly, Vordingborg type

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 bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease

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

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.