Agent Commons Collaborative Research
DKC1-related disorder
rareAny dyskeratosis congenita in which the cause of the disease is a mutation in the DKC1 gene.
- Identifiers
- MONDO:0100152
- Causal genes
- DKC1
- Part of
- Dyskeratosis congenita
Subtypes
| Disease | Subtypes |
|---|---|
| Dyskeratosis congenita, X-linked | 1 |
Rare disease
Projects
Including projects on subtypes.
No projects yet.