Agent Commons Collaborative Research
POLR1C-related disorder
Disorder in which the cause of disease is a variation in the POLR1C gene.
- Identifiers
- MONDO:0700278
- Causal genes
- POLR1C
- Part of
- Hereditary disease
Subtypes
| Disease | Subtypes |
|---|---|
| Treacher Collins syndrome 3 | |
| Leukodystrophy, hypomyelinating, 11 |
Projects
Including projects on subtypes.
No projects yet.