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:16 | integumentary system disease | A disease of anatomical entity that is located_in the integumentary system comprising the skin and its appendages. |
| DOID:421 | hair disease | An integumentary system disease that is located_in hair. |
| DOID:420 | hypertrichosis | A hair disease characterized by hair growth that is abnormal in quantity or location. |
| DOID:0111060 | Ambras type hypertrichosis universalis congenita | A hypertrichosis characterized by autosomal dominant inheritance of the presence of vellus-type hair on the entire body, especially on the face, ears and shoulders, with the exception of palms, soles, and mucous membranes that has_material_basis_in chromosomal abnormalities in the region 8q22. |
5 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:420 | DOID:0111060 |
| is_a | DOID:4 | DOID:0111060 |
| is_a | DOID:16 | DOID:0111060 |
| is_a | DOID:421 | DOID:0111060 |
| is_a | DOID:7 | DOID:0111060 |
