OMOP Concept 4154713
Congenital anomaly of endocrine gonad
StandardConditionSNOMED371118004Disorder
Maps from
1
Descendants
24
Valid from
31 Jul 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Congenital anomaly of endocrine gonad via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 371118004 | Congenital anomaly of endocrine gonad | Non-standard |
Synonyms
Alternative names recorded for Congenital anomaly of endocrine gonad across source vocabularies.
- anomalía congénita de la función endocrina gonadal
- anomalía congénita de la función endocrina gonadal (trastorno)
- Congenital anomaly of endocrine gonad (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(24)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of endocrine gland
- 1Disorder of endocrine gonad
- 1Gonadal dysgenesis
- 2Congenital malformation
- 2Congenital malformation of genital organs
- 2Disorder of endocrine system
- 2Disorder of reproductive system
- 2Genital finding
- 3Congenital disease
- 3Developmental disorder
- 3Disorder of body system
- 3Disorder of the genitourinary system
- 3Genitourinary congenital anomalies
- 3Urogenital finding
- 4Congenital anomaly of lower trunk
- 4Disease
- 4Disorder of abdominopelvic segment of trunk
- 4Disorder of fetus and/or newborn
- 4Finding of abdominopelvic segment of trunk
- 5Clinical finding
- 5Congenital abnormality of lower limb and pelvic girdle
- 5Congenital anomaly of trunk
- 5Disorder of trunk
- 5Finding of trunk structure
Narrower concepts
(24)Included automatically when you query with descendants.
- 146,XY partial gonadal dysgenesis
- 1Androgen resistance syndrome
- 1Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome
- 1Congenital anomaly of endocrine ovary
- 1Congenital anomaly of endocrine testis
- 1Frontonasal dysplasia with alopecia and genital anomaly syndrome
- 1Martsolf syndrome
- 1Ovotesticular disorder of sex development
- 246,XX ovotesticular disorder of sex development
- 246,XY ovotesticular disorder of sex development
- 2Complete androgen insensitivity syndrome
- 2Familial male-limited precocious puberty
- 2Leydig cell agenesis
- 2Ovarian dysgenesis
- 2Partial androgen insensitivity syndrome
- 2Stromal cell hyperplasia in androgen insensitivity syndrome
- 2Testicular lesion in androgen insensitivity syndrome
- 346,XX ovarian dysgenesis, short stature syndrome
- 3Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation
- 3Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation
- 3Mild androgen insensitivity syndrome
- 3Pure gonadal dysgenesis 46,XX
- 4Infertile male syndrome
- 4Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome
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