OMOP Concept 36715816
Johnson neuroectodermal syndrome
StandardConditionSNOMED721584005Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Johnson neuroectodermal syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535882 | Johnson neuroectodermal syndrome | Non-standard |
| Nebraska Lexicon | 721584005 | Alopecia, anosmia, deafness, hypogonadism syndrome | Non-standard |
Synonyms
Alternative names recorded for Johnson neuroectodermal syndrome across source vocabularies.
- Alopecia, anosmia, deafness, hypogonadism syndrome
- Johnson McMillin syndrome
- Johnson neuroectodermal syndrome (disorder)
- síndrome neuroectodérmico de Johnson
- síndrome neuroectodérmico de Johnson (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(54)Roll up to these when you need a wider cohort.
- 1Auditory system hereditary disorder
- 1Autosomal dominant hereditary disorder
- 1Congenital conductive hearing loss
- 1Developmental hereditary disorder
- 1Ectodermal dysplasia
- 1Hereditary disorder of the integument
- 1Multiple system malformation syndrome
- 2Autosomal hereditary disorder
- 2Conductive hearing loss
- 2Congenital anomaly of ear with impairment of hearing
- 2Congenital ectodermal defect
- 2Congenital malformation syndrome
- 2Decreased hearing
- 2Developmental disorder
- 2Disorder of auditory system
- 2Disorder of integument
- 2Genodermatosis
- 2Hereditary disease
- 2Hereditary disorder by system
- 3Congenital anomaly of skin
- 3Congenital hearing disorder
- 3Congenital malformation
- 3Congenital malformation of ear
- 3Decline in functional status
- 3Disease
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