OMOP Concept 4209291
Leydig cell agenesis
StandardConditionSNOMED56212008Disorder
Maps from
2
Descendants
2
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Leydig cell agenesis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 135823 | Leydig Cell Agenesis | Non-standard |
| MeSH | C562567 | Leydig Cell Hypoplasia | Non-standard |
Synonyms
Alternative names recorded for Leydig cell agenesis across source vocabularies.
- agenesia de células de Leydig
- agenesia de células de Leydig (trastorno)
- disgenesia de las células de Leydig
- Gonadotrophin unresponsiveness syndrome
- Gonadotropin unresponsiveness syndrome
- Leydig cell agenesis (disorder)
- Leydig cell dysgenesis
- Leydig cell hypoplasia
- síndrome de falta de respuesta a las gonadotrofinas
- síndrome de resistencia a las gonadotrofinas
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(51)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Congenital anomaly of endocrine testis
- 1Congenital connective tissue disorder
- 1Congenital hypoplasia of testis
- 1Connective tissue hereditary disorder
- 1Developmental hereditary disorder
- 1Hereditary disorder of endocrine system
- 1Reproductive system hereditary disorder
- 2Autosomal hereditary disorder
- 2Congenital anomaly of endocrine gonad
- 2Congenital anomaly of testis
- 2Congenital disease
- 2Congenital hypoplasia of gonad
- 2Congenital hypoplasia of testis and scrotum
- 2Developmental disorder
- 2Disorder of connective tissue
- 2Disorder of endocrine system
- 2Disorder of endocrine testis
- 2Disorder of reproductive system
- 2Hereditary disease
- 2Hereditary disorder by system
- 3Congenital anomaly of endocrine gland
- 3Congenital anomaly of male genital system
- 3Disease
- 3Disorder of body system
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Narrower concepts
(2)Included automatically when you query with descendants.
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