OMOP Concept 4031277
Amelogenesis imperfecta, hypomaturation type
StandardConditionSNOMED109475005Disorder
Maps from
1
Descendants
4
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Amelogenesis imperfecta, hypomaturation type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C536606 | Amelogenesis Imperfecta hypomaturation type | Non-standard |
Synonyms
Alternative names recorded for Amelogenesis imperfecta, hypomaturation type across source vocabularies.
- amelogénesis imperfecta - hipomaduración
- Amelogenesis imperfecta - hypomaturation
- Amelogenesis imperfecta, hypomaturation type (disorder)
- amelogénesis imperfecta, tipo hipomaduración
- amelogénesis imperfecta, tipo hipomaduración (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(42)Roll up to these when you need a wider cohort.
- 1Amelogenesis imperfecta
- 2Congenital anomaly of tooth
- 2Developmental hereditary disorder
- 2Disorder of hard tissues of teeth
- 2Hereditary disorder of tooth
- 3Congenital abnormality of oral cavity
- 3Congenital anomaly of digestive organ
- 3Congenital anomaly of jaw
- 3Developmental disorder
- 3Digestive system hereditary disorder
- 3Hereditary disease
- 3Malformation of tooth
- 3Tooth disorder
- 4Congenital anomaly of digestive system
- 4Congenital anomaly of head
- 4Congenital anomaly of mouth
- 4Congenital malformation of upper alimentary tract
- 4Disease
- 4Disorder of digestive organ
- 4Disorder of digestive system
- 4Disorder of jaw
- 4Disorder of teeth AND/OR supporting structures
- 4Disorder of tooth development
- 4Genetic disease
- 4Hereditary disorder by system
Showing 25 of 42. Retrieve the full set via the API.
Narrower concepts
(4)Included automatically when you query with descendants.
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