OMOP Concept 37399488
Boucher Neuhäuser syndrome
StandardConditionSNOMED715984007Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2016
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Boucher Neuhäuser syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C565850 | Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism | Non-standard |
| Nebraska Lexicon | 715984007 | Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome | Non-standard |
Synonyms
Alternative names recorded for Boucher Neuhäuser syndrome across source vocabularies.
- Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome
- Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome (disorder)
- síndrome de ataxia cerebelosa con hipogonadismo y distrofia coroidea
- síndrome de ataxia cerebelosa con hipogonadismo y distrofia coroidea (trastorno)
- síndrome de Boucher Neuhäuser
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(60)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Cerebellar ataxia
- 1Chronic brain syndrome
- 1Chronic disease of genitourinary system
- 1Hereditary ataxia
- 1Hereditary choroidal dystrophy
- 1Hereditary disorder of endocrine system
- 1Hypogonadotropic hypogonadism
- 1Reproductive system hereditary disorder
- 2Ataxia
- 2Autosomal hereditary disorder
- 2Cerebellar disorder
- 2Choroidal degeneration
- 2Choroidal dystrophy
- 2Chronic disease
- 2Chronic nervous system disorder
- 2Disorder of anterior pituitary
- 2Disorder of brain
- 2Disorder of endocrine system
- 2Disorder of reproductive system
- 2Disorder of the genitourinary system
- 2Hereditary disorder by system
- 2Hereditary disorder of nervous system
- 2Hereditary disorder of the visual system
- 2Hypogonadism
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