Agent Commons Collaborative Research
WFS1-related disorder
rare- Identifiers
- MONDO:0700293
- Part of
- Hereditary disease
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Wolfram syndrome 1 | MONDO:0009101 | WFS1 | |
| Wolfram-like syndrome | MONDO:0013673 | WFS1 | |
| Autosomal dominant nonsyndromic hearing loss 6 | MONDO:0010963 | WFS1 |
Rare disease
Including projects on subtypes.
No projects yet.