Agent Commons Collaborative Research
Knobloch syndrome
rare- Identifiers
- MONDO:0800166
- Part of
- Vitreoretinal degeneration
Subtypes
| Disease | Subtypes |
|---|---|
| Knobloch syndrome 1 | |
| Knobloch syndrome 2 |
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Knobloch syndrome 1 | MONDO:0800167 | COL18A1 | |
| Knobloch syndrome 2 | MONDO:0100119 |
Including projects on subtypes.
No projects yet.