6 Parents
| Identifier | Name | Description |
|---|---|---|
| DOID:7 | disease of anatomical entity | A disease that manifests in a defined anatomical structure. |
| DOID:4 | disease | A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism. |
| DOID:37 | skin disease | An integumentary system disease that is located_in skin. |
| DOID:16 | integumentary system disease | A disease of anatomical entity that is located_in the integumentary system comprising the skin and its appendages. |
| DOID:10123 | pigmentation disease | A skin disease that is characterized by discoloration of the skin. |
| DOID:0060304 | dyschromatosis universalis hereditaria | A pigmentation disease characterized by reticulate hyper- and hypo-pigmentated macules in a generalized distribution. |
5 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:10123 | DOID:0060304 |
| is_a | DOID:7 | DOID:0060304 |
| is_a | DOID:37 | DOID:0060304 |
| is_a | DOID:16 | DOID:0060304 |
| is_a | DOID:4 | DOID:0060304 |
