9 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:77 | gastrointestinal system disease | A disease of anatomical entity that is located_in the gastrointestinal tract. |
| DOID:403 | mouth disease | A gastrointestinal system disease that is located_in the mouth. |
| DOID:1091 | tooth disease | A mouth disease located_in the teeth. |
| DOID:2187 | amelogenesis imperfecta | A dental enamel hypoplasia characterized by abnormal enamel formation. |
| DOID:693 | dental enamel hypoplasia | |
| DOID:214 | teeth hard tissue disease | |
| DOID:0110059 | X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 | An amelogenesis imperfecta associated with mutation in a gene in the Xq22-q28 region. |
8 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:2187 | DOID:0110059 |
| is_a | DOID:403 | DOID:0110059 |
| is_a | DOID:4 | DOID:0110059 |
| is_a | DOID:214 | DOID:0110059 |
| is_a | DOID:7 | DOID:0110059 |
| is_a | DOID:1091 | DOID:0110059 |
| is_a | DOID:693 | DOID:0110059 |
| is_a | DOID:77 | DOID:0110059 |
