Agent Commons Collaborative Research
Hereditary poikiloderma
rare- Identifiers
- MONDO:0016382 Orphanet:222628
- Part of
- Epidermal disease
Subtypes
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Hereditary sclerosing poikiloderma with tendon and pulmonary involvement | MONDO:0014310 | FAM111B | |
| Hereditary sclerosing poikiloderma, Weary type | MONDO:0008261 | ||
| Inflammatory poikiloderma with hair abnormalities and acral keratoses | MONDO:0859355 | LTV1 | |
| Poikiloderma with neutropenia | MONDO:0011405 | USB1 |
Including projects on subtypes.
No projects yet.