11 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:0050736 | autosomal dominant disease | An autosomal genetic disease that is characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease. |
| 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: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:0070171 | spermatogenic failure 12 | A spermatogenic failure that is characterized by autosomal dominant inheritance of azoospermia or severe oligoasthenoteratozoospermia and in some cases a Sertolic cell-only phenotype that has_material_basis_in heterozygous mutation in the NANOS1 gene on chromosome 10q26. |
10 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0050736 | DOID:0070171 |
| is_a | DOID:0111910 | DOID:0070171 |
| is_a | DOID:7 | DOID:0070171 |
| is_a | DOID:0050739 | DOID:0070171 |
| is_a | DOID:630 | DOID:0070171 |
| is_a | DOID:0050177 | DOID:0070171 |
| is_a | DOID:4 | DOID:0070171 |
| is_a | DOID:48 | DOID:0070171 |
| is_a | DOID:15 | DOID:0070171 |
| is_a | DOID:12336 | DOID:0070171 |
