Rubinstein-Taybi syndrome due to CREBBP mutations |
Polysyndactyly, unilateral |
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INTERACTOME ASSOCIATIONS (click on a score value to see the evidence) |
CREBBP
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Citations in the biomedical literature:
Rubinstein-Taybi syndrome due to CREBBP mutations |
Polysyndactyly, unilateral |
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Synonym(s): (no synonyms)
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Synonym(s): - Preaxial polydactyly type 4, unilateral
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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
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Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease
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Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -
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Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -
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Epidemiological data: (no data available)
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Epidemiological data: (no data available)
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External references: 1 OMIM reference -
No MeSH references | |
External references: No OMIM references No MeSH references
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No signs/symptoms info available.