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:28 | endocrine system disease | A disease of anatomical entity that is located_in endocrine glands which secretes a type of hormone directly into the bloodstream to regulate the body. |
| DOID:2277 | gonadal disease | An endocrine system disease that is located_in the gonads. |
| DOID:1923 | disorder of sexual development | A gonadal disease that is characterized by atypical development of chromosomal, gonadal, or anatomic sex. |
| DOID:4674 | androgen insensitivity syndrome | A disorder of sexual development that is characterized by the inability of the cell to respond to androgens in individuals with a karyotype of 46,XY resulting in female physical traits but male genetic makeup. |
| DOID:0080775 | complete androgen insensitivity syndrome | An androgen insensitivity syndrome that is characterized by complete androgen insensitivity as the body cannot use androgens at all, having the external sex characteristics of females but no uterus. |
6 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:4674 | DOID:0080775 |
| is_a | DOID:1923 | DOID:0080775 |
| is_a | DOID:28 | DOID:0080775 |
| is_a | DOID:4 | DOID:0080775 |
| is_a | DOID:2277 | DOID:0080775 |
| is_a | DOID:7 | DOID:0080775 |
