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Synpolydactyly type 1
1 OMIM reference -
1 associated gene
7 connected diseases
No signs/symptoms info
Disease Type of connection
Brachydactyly type E
Brachydactyly-syndactyly, Zhao type
Syndactyly type 5
VACTERL / VATER association
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
Synonym(s):
- SD2, Vordingborg type
- SD2a
- SPD, Vordingborg type
- SPD1
- Synpolydactyly, Vordingborg type
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
HOXD13 P35453142989
No signs/symptoms info available.