OMOP Concept 4127740
Congenitally impaired spermatogenesis
StandardConditionSNOMED236799006Disorder
Maps from
1
Descendants
2
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Congenitally impaired spermatogenesis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 236799006 | Congenitally impaired spermatogenesis | Non-standard |
Synonyms
Alternative names recorded for Congenitally impaired spermatogenesis across source vocabularies.
- afección espermatogénica congénita
- afección espermatogénica congénita (trastorno)
- Congenitally impaired spermatogenesis (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(28)Roll up to these when you need a wider cohort.
- 1Congenital male infertility
- 1Disorder of testis
- 2Congenital disease
- 2Disorder of male genital organ
- 2Primary male infertility
- 2Testicular finding
- 3Disorder of fetus and/or newborn
- 3Disorder of male reproductive system
- 3Male genitalia finding
- 3Male infertility
- 4Disease
- 4Disorder of pelvic region of trunk
- 4Disorder of reproductive system
- 4Finding of pelvic region of trunk
- 4Genital finding
- 4Infertile
- 5Clinical finding
- 5Disorder of abdominopelvic segment of trunk
- 5Disorder of the genitourinary system
- 5Fertility problem
- 5Finding of abdominopelvic segment of trunk
- 5Urogenital finding
- 6Disorder of body system
- 6Disorder of trunk
- 6Finding of fertility
Narrower concepts
(2)Included automatically when you query with descendants.
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