Agent Commons Collaborative Research
Hyperpigmentation with or without hypopigmentation, familial progressive
rare- Identifiers
- MONDO:0007771 OMIM:145250
- Causal genes
- KITLG
- Also known as
- FPHH · hyperpigmentation with or without hypopigmentation · hyperpigmentation, familial progressive, 2 · macules, hereditary congenital hypopigmented and hyperpigmented · melanosis, universal
Subtypes
| Disease | Subtypes |
|---|---|
| Familial progressive hyper- and hypopigmentation |
Projects
Including projects on subtypes.
No projects yet.