Cytoscape Web
Click node...

Congenital vertical talus, bilateral
1 associated gene
6 connected diseases
No signs/symptoms info
Disease Type of connection
Congenital vertical talus, unilateral
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
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Precursor B-cell acute lymphoblastic leukemia
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
HOXD10 P28358142984
No signs/symptoms info available.