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:48 | male reproductive system disease | A reproductive system disease that affects male reproductive organs. |
| DOID:15 | reproductive system disease | A disease of anatomical entity that is located_in reproductive system organs. |
| 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:12336 | male infertility | |
| DOID:0050457 | Sertoli cell-only syndrome | A male infertility disease characterized by male sterility, has_material_basis_in azospermia without abnormal sexual development. |
| DOID:0060388 | chromosomal deletion syndrome | A chromosomal disease that has_material_basis_in partial deletion of chromosomes. |
| DOID:0080014 | chromosomal disease | A genetic disease that has_material_basis_in extra, missing, or re-arranged chromosomes. |
| DOID:0050738 | Y-linked monogenic disease | A monogenic disease that has_material_basis_in mutations on the Y chromosome. |
| DOID:0070186 | Y-linked spermatogenic failure 1 | A Sertoli cell-only syndrome that has_material_basis_in deletions in the Yq11 chromosomal region. |
11 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0050457 | DOID:0070186 |
| is_a | DOID:0060388 | DOID:0070186 |
| is_a | DOID:0050738 | DOID:0070186 |
| is_a | DOID:7 | DOID:0070186 |
| is_a | DOID:48 | DOID:0070186 |
| is_a | DOID:15 | DOID:0070186 |
| is_a | DOID:12336 | DOID:0070186 |
| is_a | DOID:630 | DOID:0070186 |
| is_a | DOID:4 | DOID:0070186 |
| is_a | DOID:0080014 | DOID:0070186 |
| is_a | DOID:0050177 | DOID:0070186 |
