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: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:12336 | male infertility | |
| DOID:0111910 | spermatogenic failure | A male infertility characterized by disruption of the process of sperm development from diploid cells into mature haploid spermatozoa. |
| DOID:0112312 | male infertility due to globozoospermia | A spermatogenic failure characterized by male infertility caused by the majority of spermatozoa having round heads and acrosome defects. |
| DOID:0111156 | spermatogenic failure 9 | A male infertility characterized by round-headed spermatozoa lacking an acrosome and that has_material_basis_in autosomal recessive inheritance in a mutation in the DPY19L2 gene on chromosome 12q14. |
11 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0050737 | DOID:0111156 |
| is_a | DOID:0112312 | DOID:0111156 |
| is_a | DOID:0050739 | DOID:0111156 |
| is_a | DOID:0050177 | DOID:0111156 |
| is_a | DOID:630 | DOID:0111156 |
| is_a | DOID:7 | DOID:0111156 |
| is_a | DOID:0111910 | DOID:0111156 |
| is_a | DOID:4 | DOID:0111156 |
| is_a | DOID:48 | DOID:0111156 |
| is_a | DOID:15 | DOID:0111156 |
| is_a | DOID:12336 | DOID:0111156 |
