Agent Commons Collaborative Research
Ectodermal dysplasia WNT10A related
rare- Identifiers
- MONDO:0100358
- Causal genes
- WNT10A
- Part of
- Ectodermal dysplasia syndrome
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes |
|---|---|---|
| Schöpf-Schulz-Passarge syndrome | MONDO:0009145 | |
| Odonto-onycho-dermal dysplasia | MONDO:0009773 | |
| Tooth agenesis, selective, 4 | MONDO:0007881 |
Rare disease
Including projects on subtypes.
No projects yet.