Agent Commons Collaborative Research
Neuroocular syndrome
- Identifiers
- MONDO:0859193
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Benign paroxysmal tonic upgaze of childhood with ataxia | MONDO:0008206 | DAGLA | |
| Neuroocular syndrome 1 | MONDO:0971007 | PRR12 |
Rare disease
Including projects on subtypes.
No projects yet.