OMOP Concept 4126774
Amelogenesis imperfecta - hypoplastic autosomal dominant - local
StandardConditionSNOMED234961008Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Amelogenesis imperfecta - hypoplastic autosomal dominant - local via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C562879 | Amelogenesis Imperfecta, Type IB | Non-standard |
| Nebraska Lexicon | 234961008 | Amelogenesis imperfecta - hypoplastic autosomal dominant - local | Non-standard |
Synonyms
Alternative names recorded for Amelogenesis imperfecta - hypoplastic autosomal dominant - local across source vocabularies.
- amelogénesis imperfecta hipoplásica, autosómica dominante, local
- amelogénesis imperfecta hipoplásica, autosómica dominante, local (trastorno)
- Amelogenesis imperfecta - hypoplastic autosomal dominant - local (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(45)Roll up to these when you need a wider cohort.
- 1Amelogenesis imperfecta, hypoplastic type
- 1Autosomal dominant hereditary disorder
- 2Amelogenesis imperfecta
- 2Autosomal hereditary disorder
- 3Congenital anomaly of tooth
- 3Developmental hereditary disorder
- 3Disorder of hard tissues of teeth
- 3Hereditary disease
- 3Hereditary disorder of tooth
- 4Congenital abnormality of oral cavity
- 4Congenital anomaly of digestive organ
- 4Congenital anomaly of jaw
- 4Developmental disorder
- 4Digestive system hereditary disorder
- 4Genetic disease
- 4Malformation of tooth
- 4Tooth disorder
- 5Congenital anomaly of digestive system
- 5Congenital anomaly of head
- 5Congenital anomaly of mouth
- 5Disease
- 5Disorder of digestive organ
- 5Disorder of digestive system
- 5Disorder of jaw
- 5Disorder of teeth AND/OR supporting structures
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