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loading...| Preferred Name | Azoospermia, Nonobstructive | |
| Synonyms |
|
|
| ID |
http://purl.bioontology.org/ontology/MESH/C564665 |
|
| cui |
C1847540 |
|
| HM |
D053713 |
|
| Inverse of RB |
0 |
|
| Mapped to | ||
| MDA |
20121105 |
|
| MeSH Frequency |
407 |
|
| MMR |
20190618 |
|
| notation |
C564665 |
|
| prefLabel |
Azoospermia, Nonobstructive |
|
| SC |
3 |
|
| Scope Statement |
Azoospermia that is caused by hereditary defects which disrupt sperm development before or during meiosis. Mutations and polymorphisms in the USP9Y (OMIM: 415000), SLC26A8 (OMIM: 606766), DAZL (OMIM: 601486), and SYCP3 (OMIM: 270960) have been identified. |
|
| TERMUI |
T805361 |
|
| TH |
OMIM (2013) |
|
| tui |
T047 |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/OMIM/MTHU062438 | OMIM | CUI | |
| http://purl.bioontology.org/ontology/OMIM/MTHU055533 | OMIM | CUI | |
| http://phenomebrowser.net/ontologies/mesh/mesh.owl#C564665 | RH-MESH | LOOM | |
| http://purl.bioontology.org/ontology/OMIM/MTHU055533 | OMIM | LOOM |