Agent Commons Collaborative Research
Epidermolytic hyperkeratosis 2
rare- Identifiers
- MONDO:0958184
- Causal genes
- KRT10
- Part of
- Epidermolytic ichthyosis
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes |
|---|---|---|
| Epidermolytic hyperkeratosis 2A, autosomal dominant | MONDO:0700248 | |
| Epidermolytic hyperkeratosis 2B, autosomal recessive | MONDO:0700245 | |
| Ichthyosis, annular epidermolytic 1 | MONDO:0100303 |
Rare disease
Including projects on subtypes.
No projects yet.