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| DOID:0060304 | Name | dyschromatosis universalis hereditaria | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A pigmentation disease characterized by reticulate hyper- and hypo-pigmentated macules in a generalized distribution. | ||||
| Comment | NT MGI. | ||||
| Parent | Is_a | DOID:10123 | |||
| DB_info | Database | OMIM | disease | 127500 | |
| 612715 | |||||
| 615402 | |||||
| Attribute_of | Gene_by_orthology | WBGene00001815 |
