OMOP Concept 4031276
Amelogenesis imperfecta, hypocalcification type
StandardConditionSNOMED109471001Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Amelogenesis imperfecta, hypocalcification type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C562880 | Amelogenesis Imperfecta, Type III | Non-standard |
Synonyms
Alternative names recorded for Amelogenesis imperfecta, hypocalcification type across source vocabularies.
- amelogénesis imperfecta hipocalcificada
- amelogénesis imperfecta hipomineralizada
- Amelogenesis imperfecta, hypocalcification type (disorder)
- Amelogenesis imperfecta - hypocalcified
- Amelogenesis imperfecta - hypomineralisation
- Amelogenesis imperfecta - hypomineralization
- amelogénesis imperfecta, tipo hipocalcificación
- amelogénesis imperfecta, tipo hipocalcificación (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(47)Roll up to these when you need a wider cohort.
- 1Amelogenesis imperfecta
- 1Hypomineralization of enamel of teeth
- 2Congenital anomaly of tooth
- 2Developmental hereditary disorder
- 2Disorder of hard tissues of teeth
- 2Hereditary disorder of tooth
- 2Hypocalcification of teeth
- 2Hypomineralization of enamel of tooth
- 3Congenital abnormality of oral cavity
- 3Congenital anomaly of digestive organ
- 3Congenital anomaly of jaw
- 3Developmental disorder
- 3Digestive system hereditary disorder
- 3Finding of dentition
- 3Hereditary disease
- 3Hypomineralization of tooth
- 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
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