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Postaxial polydactyly type B, bilateral
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
2 associated genes
No signs/symptoms info
Postaxial polydactyly type B, bilateral
Acute myeloid leukemia with t(8;16)(p11;p13) translocation

GLI3
(UniProt - OMIM)
 CREBBP
(UniProt - OMIM)
KAT6A
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
GLI3
(0.88)
CREBBP


Citations in the biomedical literature:


Postaxial polydactyly type B, bilateral
GLI3
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
CREBBP KAT6A



Postaxial polydactyly type B, bilateral
Acute myeloid leukemia with t(8;16)(p11;p13) translocation

Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic 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:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.