dyschromatosis universalis hereditaria
MeSH: C535730ORPHA: 241
Overview
pigmentation disease characterized by reticulate hyper- and hypo-pigmentated macules in a generalized distribution
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with dyschromatosis universalis hereditaria, sourced from HPO and Orphanet clinical annotations.
Hearing impairmentCutaneous photosensitivityHypermelanotic maculeHypopigmented skin patchesFrecklingShort statureSpotty hypopigmentationMultiple cafe-au-lait spotsMacule
Classification & Codes
MeSH Code
C535730Orphanet Code
ORPHA:241dyschromatosis universalis hereditaria
| MeSH | C535730 |
| Orphanet | ORPHA:241 |
| Treatments | 0 drug(s) |
| Symptoms on record | 9 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO