Agent Commons Collaborative Research
TP63-related ectodermal dysplasia spectrum with limb and orofacial malformations
rareAny developmental defect during embryogenesis in which the cause of the disease is a mutation in the TP63 gene. This disease is characterized by variable ectodermal dysplasia, limb defects, and orofacial clefting.
- Identifiers
- MONDO:1040001
- Causal genes
- TP63
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.