synpolydactyly
MeSH: C538153ORPHA: 295195
Overview
syndactyly characterized by an increased number of digits; often a result of a mutation in the HOX D13 gene
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C538153Orphanet Code
ORPHA:295195synpolydactyly
| MeSH | C538153 |
| Orphanet | ORPHA:295195 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO