OMOP Concept 36714610
Trichodysplasia with amelogenesis imperfecta syndrome
StandardConditionSNOMED719911000Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Trichodysplasia with amelogenesis imperfecta syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 719911000 | Trichodysplasia with amelogenesis imperfecta syndrome | Non-standard |
Synonyms
Alternative names recorded for Trichodysplasia with amelogenesis imperfecta syndrome across source vocabularies.
- síndrome de tricodisplasia con amelogénesis imperfecta
- síndrome de tricodisplasia con amelogénesis imperfecta (trastorno)
- Trichodysplasia with amelogenesis imperfecta syndrome (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(61)Roll up to these when you need a wider cohort.
- 1Amelogenesis imperfecta
- 1Ectodermal dysplasia
- 1Hereditary disorder of the integument
- 1X-linked recessive hereditary disease
- 2Congenital anomaly of tooth
- 2Congenital ectodermal defect
- 2Developmental hereditary disorder
- 2Disorder of hard tissues of teeth
- 2Disorder of integument
- 2Genodermatosis
- 2Hereditary disorder by system
- 2Hereditary disorder of tooth
- 2X-linked hereditary disease
- 3Congenital abnormality of oral cavity
- 3Congenital anomaly of digestive organ
- 3Congenital anomaly of jaw
- 3Congenital anomaly of skin
- 3Congenital malformation
- 3Developmental disorder
- 3Digestive system hereditary disorder
- 3Disorder of body system
- 3Disorder of embryonic structure
- 3Hereditary disease
- 3Integumentary system finding
- 3Malformation of tooth
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