OMOP Concept 4167354
Hypogonadism
StandardConditionSNOMED48130008Disorder
Maps from
5
Descendants
102
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
5 source codes normalize to Hypogonadism via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 113366 | Hereditary familial hypogonadism with hypospadias and gynecomastia | Non-standard |
| CIEL | 117346 | Hypogonadism | Non-standard |
| HPO | HP_0000135 | Hypogonadism | Non-standard |
| MeSH | D007006 | Hypogonadism | Non-standard |
| Nebraska Lexicon | 48130008 | Hypogonadism | Non-standard |
Synonyms
Alternative names recorded for Hypogonadism across source vocabularies.
- hipogonadismo
- hipogonadismo (trastorno)
- Hypogonadism (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(13)Roll up to these when you need a wider cohort.
- 1Disorder of endocrine gonad
- 2Disorder of endocrine system
- 2Disorder of reproductive system
- 2Genital finding
- 3Disorder of body system
- 3Disorder of the genitourinary system
- 3Urogenital finding
- 4Disease
- 4Disorder of abdominopelvic segment of trunk
- 4Finding of abdominopelvic segment of trunk
- 5Clinical finding
- 5Disorder of trunk
- 5Finding of trunk structure
Narrower concepts
(102)Included automatically when you query with descendants.
- 1Congenital cataract with deafness and hypogonadism syndrome
- 1Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome
- 1Deafness and hypogonadism syndrome
- 1Female hypogonadism syndrome
- 1Frontonasal dysplasia with alopecia and genital anomaly syndrome
- 1Gonad postablative failure
- 1Hypogonadal obesity
- 1Hypogonadotropic hypogonadism
- 1Male hypogonadism
- 1Microcephalic primordial dwarfism, insulin resistance syndrome
- 1Primary hypogonadism
- 1Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome
- 1Scholte syndrome
- 1Syndromic X-linked intellectual disability type 7
- 24H leukodystrophy
- 2Acquired testicular failure
- 2Adiposogenital dystrophy
- 2Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome
- 2Boucher Neuhäuser syndrome
- 2Congenital hypogonadotropic hypogonadism
- 2Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome
- 2Eunuchoid gigantism
- 2Female hypogonadotropic hypogonadism
- 2Functional hypogonadotropic hypogonadism
- 2Hydrocephalus with obesity and hypogonadism syndrome
- 2Hypergonadotropic hypogonadism with cataract syndrome
- 2Hypogonadism with mitral valve prolapse and intellectual disability syndrome
- 2Hypogonadism with prune belly syndrome
- 2Hypogonadotropic hypogonadism due to follicle-stimulating hormone deficiency
- 2Hypogonadotropic hypogonadism due to isolated gonadotropin deficiency
- 2Hypogonadotropic hypogonadism due to luteinizing hormone deficiency
- 2Idiopathic hypogonadotropic hypogonadism
- 2Induced male hypogonadism syndrome
- 2Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome
- 2Microcephalus, hypergonadotropic hypogonadism, short stature syndrome
- 2Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome
- 2Ovarian failure
- 2Polyendocrine polyneuropathy syndrome
- 2Primary hypergonadotropic hypogonadism and partial alopecia syndrome
- 2Primary ovarian failure
- 2Primary testicular failure
- 2Progressive cerebellar ataxia with hypogonadism
- 2Testicular hypofunction
- 2Woodhouse Sakati syndrome
- 2X-linked intellectual disability Cilliers type
- 2X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome
- 2X-linked intellectual disability Van Esch type
- 3Alopecia, progressive neurological defect, endocrinopathy syndrome
- 3Autoimmune primary ovarian failure
- 3Congenital leptin deficiency
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