Witkop syndrome [Supplementary Concept]
Autosomal dominant disorder characterized by nail dysplasia and congenitally missing permanent teeth; associated with mutations in the MSX1 gene
Date introduced: August 25, 2010
MeSH Unique ID: C536736
Heading Mapped to:
Entry Terms:
- Dysplasia of nails with hypodontia
- Tooth and nail syndrome
- Nail Dysplasia With Hypodontia
- Tooth-And-Nail Syndrome