OMOP Concept 4153218
Primary hypogonadism
StandardConditionSNOMED370999003Disorder
Maps from
1
Descendants
30
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 Primary hypogonadism via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| HPO | HP_0000815 | Hypergonadotropic hypogonadism | Non-standard |
Synonyms
Alternative names recorded for Primary hypogonadism across source vocabularies.
- hipogonadismo hipergonadotrófico
- hipogonadismo primario
- hipogonadismo primario (trastorno)
- Hypergonadotropic hypogonadism
- Primary hypogonadism (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(14)Roll up to these when you need a wider cohort.
- 1Hypogonadism
- 2Disorder of endocrine gonad
- 3Disorder of endocrine system
- 3Disorder of reproductive system
- 3Genital finding
- 4Disorder of body system
- 4Disorder of the genitourinary system
- 4Urogenital finding
- 5Disease
- 5Disorder of abdominopelvic segment of trunk
- 5Finding of abdominopelvic segment of trunk
- 6Clinical finding
- 6Disorder of trunk
- 6Finding of trunk structure
Narrower concepts
(30)Included automatically when you query with descendants.
- 1Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome
- 1Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome
- 1Hydrocephalus with obesity and hypogonadism syndrome
- 1Hypergonadotropic hypogonadism with cataract syndrome
- 1Hypogonadism with mitral valve prolapse and intellectual disability syndrome
- 1Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome
- 1Microcephalus, hypergonadotropic hypogonadism, short stature syndrome
- 1Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome
- 1Primary hypergonadotropic hypogonadism and partial alopecia syndrome
- 1Primary ovarian failure
- 1Primary testicular failure
- 1Woodhouse Sakati syndrome
- 1X-linked intellectual disability Cilliers type
- 1X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome
- 1X-linked intellectual disability Van Esch type
- 2Autoimmune primary ovarian failure
- 2Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome
- 2Ovarian dysgenesis
- 2Premature ovarian insufficiency
- 2Resistant ovary syndrome
- 346,XX ovarian dysgenesis, short stature syndrome
- 3Fragile X associated primary ovarian insufficiency
- 3Iatrogenic premature ovarian insufficiency
- 3Idiopathic premature ovarian insufficiency
- 3Ovarioleukodystrophy
Showing 25 of 30. Retrieve the full set via the API.
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