12 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:0050177 | monogenic disease | A genetic disease that is the result of one or more abnormal alleles and may be dominant, semi-dominant, or recessive. |
| DOID:630 | genetic disease | A disease that has_material_basis_in genetic variations in the human genome. |
| DOID:0050739 | autosomal genetic disease | A monogenic disease that has_material_basis_in a mutation in a single gene on one of the non-sex chromosomes. |
| DOID:0050737 | autosomal recessive disease | An autosomal genetic disease that is characterized by the presence of two mutated copies of the gene, both of which must be present in order for the disease or trait to develop. |
| 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:14447 | gonadal dysgenesis | A disorder of sexual development that is characterized by a progressive loss of germ cells on the developing gonads of an embryo. |
| DOID:14448 | 46,XY sex reversal | A gonadal dysgenesis that is characterized by a normal 46,XY karyotype along with a progressive loss of germ cells on the developing gonads of an embryo. |
| DOID:0111773 | 46,XY sex reversal 8 | A 46 XY sex reversal characterized by an XY karyotype, phenotypically female genitalia and failure to develop secondary sexual characteristics at puberty including menstruation that has_material_basis_in homozygous or compound heterozygous mutation in the AKR1C2 gene on chromosome 10p15.1. |
11 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:14448 | DOID:0111773 |
| is_a | DOID:0050737 | DOID:0111773 |
| is_a | DOID:0050739 | DOID:0111773 |
| is_a | DOID:28 | DOID:0111773 |
| is_a | DOID:7 | DOID:0111773 |
| is_a | DOID:630 | DOID:0111773 |
| is_a | DOID:2277 | DOID:0111773 |
| is_a | DOID:0050177 | DOID:0111773 |
| is_a | DOID:4 | DOID:0111773 |
| is_a | DOID:14447 | DOID:0111773 |
| is_a | DOID:1923 | DOID:0111773 |
