OMOP Concept 4132094
Disorder of endocrine gonad
StandardConditionSNOMED127345001Disorder
Maps from
2
Descendants
204
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Disorder of endocrine gonad via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 135821 | Leydig Cell Hyperplasia | Non-standard |
| Nebraska Lexicon | 127345001 | Disorder of endocrine gonad | Non-standard |
Synonyms
Alternative names recorded for Disorder of endocrine gonad across source vocabularies.
- Disorder of endocrine gonad (disorder)
- trastorno de las gónadas endocrinas
- trastorno de las gónadas endocrinas (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(12)Roll up to these when you need a wider cohort.
- 1Disorder of endocrine system
- 1Disorder of reproductive system
- 1Genital finding
- 2Disorder of body system
- 2Disorder of the genitourinary system
- 2Urogenital finding
- 3Disease
- 3Disorder of abdominopelvic segment of trunk
- 3Finding of abdominopelvic segment of trunk
- 4Clinical finding
- 4Disorder of trunk
- 4Finding of trunk structure
Narrower concepts
(204)Included automatically when you query with descendants.
- 1Complex gonadal endocrine disorder
- 1Congenital anomaly of endocrine gonad
- 1Disorder of endocrine ovary
- 1Disorder of endocrine testis
- 1Disorder of sexual differentiation
- 1Endocrine andrology disorder
- 1Endocrine disorder related to puberty
- 1Gynecological endocrinology disorder
- 1Hypergonadism
- 1Hypogonadism
- 1Precocious puberty
- 1Puberty disorder due to estrogen resistance
- 246,XY partial gonadal dysgenesis
- 2Acquired male infertility of endocrine origin
- 2Androgen resistance syndrome
- 2Central precocious puberty
- 2Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome
- 2Congenital anomaly of endocrine ovary
- 2Congenital anomaly of endocrine testis
- 2Congenital cataract with deafness and hypogonadism syndrome
- 2Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome
- 2Corpus albicans cyst of ovary
- 2Corpus luteum cyst
- 2Corpus luteum deficiency syndrome
- 2Cryptogenic sexual precocity
- 2Cycling ovulatory disorder
- 2Deafness and hypogonadism syndrome
- 2Disorder of androgen receptor
- 2Disorder of testicular differentiation AND/OR development
- 2Empty follicle syndrome
- 2Endocrine female infertility
- 2Endocrine menstrual disturbance
- 2Eunuchism
- 2Familial male-limited precocious puberty
- 2Female hypogonadism syndrome
- 2Frontonasal dysplasia with alopecia and genital anomaly syndrome
- 2Galactorrhea not associated with childbirth
- 2Gonadotropin independent precocious puberty
- 2Gonad postablative failure
- 2Hyperandrogenism due to non-classic 21-hydroxylase deficiency
- 2Hyperandrogenization syndrome
- 2Hypogonadal obesity
- 2Hypogonadotropic hypogonadism
- 2Isosexual precocious puberty
- 2Isosexual virilization
- 2Leydig cell hyperplasia of ovary
- 2Leydig cell hyperplasia of testis
- 2Luteal phase defect
- 2Luteinized unruptured follicle syndrome
- 2Male hypogonadism
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