7 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:161 | keratosis | A skin disease characterized_by growth of keratin on the skin or mucous membranes. |
| DOID:869 | cholesteatoma | A keratosis that is characterized by keratinizing squamous epithelium located in middle ear and/or mastoid, subepithelial connective tissue and by the progressive accumulation of keratin debris with or without surrounding inflammatory reaction. |
| DOID:0060360 | hereditary papulotranslucent acrokeratoderma | A keratosis of the hands and feet characterized by persistent, asymptomatic, yellowish to white papules and plaques associated with fine-textured scalp hair and an atopic diathesis. |
6 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:869 | DOID:0060360 |
| is_a | DOID:7 | DOID:0060360 |
| is_a | DOID:16 | DOID:0060360 |
| is_a | DOID:4 | DOID:0060360 |
| is_a | DOID:37 | DOID:0060360 |
| is_a | DOID:161 | DOID:0060360 |
