Disease Browser
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Parent Node: Infertility, Male (D007248) | ..Starting node ..Azoospermia (D053713)
| Child Nodes:
| ........Azoospermia, Nonobstructive (C564665) | ........Incomplete Sertoli Cell-Only Syndrome (C564033) | ........SPERMATOGENIC FAILURE 4 (OMIM:270960) | ........Y Chromosome Infertility (C580551) |
Sister Nodes: | ..Aromatase deficiency (C537436)
| ..Aspermia (D053714)
| ..Asthenozoospermia (D053627) 1
| ..Azoospermia (D053713) 4
| ..Catsper1-Related Nonsyndromic Male Infertility (C579978)
| ..Deafness, Sensorineural, And Male Infertility (C567010)
| ..Familial gynecomastia, due to increased aromatase activity (C000591739)
| ..Male Infertility with Large-Headed, Multiflagellar, Polyploid Spermatozoa (C562903)
| ..Oligospermia (D009845) 3
| ..Oligosynaptic Infertility (C562902)
| ..Sertoli Cell-Only Syndrome (D054331) 2
| ..SPERMATOGENIC FAILURE 2 (OMIM:108420)
| ..SPERMATOGENIC FAILURE 6 (OMIM:102530)
| ..Spermatogenic Failure, Nonobstructive, Y-Linked (C564030)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 1115 |
Name: | Azoospermia |
Definition: | A condition of having no sperm present in the ejaculate (SEMEN). |
Alternative IDs: | |
ParentIDs: | MESH:D007248 |
TreeNumbers: | C12.294.365.700.380 |
Synonyms: | |
Slim Mappings: | Urogenital disease (male) |
Reference: |
MedGen: D053713
MeSH: D053713
OMIM:
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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