OMOP Concept 36716769
Congenital hypogonadotropic hypogonadism
StandardConditionSNOMED722944006Disorder
Maps from
1
Descendants
19
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Congenital hypogonadotropic hypogonadism via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 722944006 | Congenital hypogonadotropic hypogonadism | Non-standard |
Synonyms
Alternative names recorded for Congenital hypogonadotropic hypogonadism across source vocabularies.
- Congenital hypogonadotropic hypogonadism (disorder)
- hipogonadismo hipogonadotrófico congénito
- hipogonadismo hipogonadotrófico congénito (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(27)Roll up to these when you need a wider cohort.
- 1Congenital disease
- 1Hypogonadotropic hypogonadism
- 2Disorder of anterior pituitary
- 2Disorder of fetus and/or newborn
- 2Hypogonadism
- 2Hypopituitarism
- 3Disease
- 3Disorder of endocrine gonad
- 3Disorder of pituitary gland
- 4Clinical finding
- 4Disorder of brain
- 4Disorder of endocrine system
- 4Disorder of reproductive system
- 4Genital finding
- 5Disorder of body system
- 5Disorder of head
- 5Disorder of the central nervous system
- 5Disorder of the genitourinary system
- 5Finding of brain
- 5Urogenital finding
- 6Central nervous system finding
- 6Disorder of abdominopelvic segment of trunk
- 6Disorder of nervous system
- 6Finding of abdominopelvic segment of trunk
- 6Head finding
Narrower concepts
(19)Included automatically when you query with descendants.
- 1Alopecia, progressive neurological defect, endocrinopathy syndrome
- 1Congenital leptin deficiency
- 1Familial adrenal hypoplasia with absent pituitary luteinizing hormone
- 1Hypogonadism with anosmia
- 1Hypogonadotropic hypogonadism retinitis pigmentosa syndrome
- 1Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome
- 1Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome
- 1Hyposmia, nasal and ocular hypoplasia, hypogonadotropic hypogonadism syndrome
- 1Intellectual disability, myopathy, short stature, endocrine defect syndrome
- 1Martsolf syndrome
- 1Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome
- 1Obesity due to leptin receptor gene deficiency
- 1Prader-Willi-like syndrome
- 1Prader-Willi syndrome
- 26q16 microdeletion syndrome
- 2CPE-related Prader-Willi-like syndrome
- 2Kallman syndrome with heart disease
- 2MAGEL2-related Prader-Willi-like syndrome
- 2SIM1-related Prader-Willi-like syndrome
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