OMOP Concept 36713640
Acromesomelic dysplasia Maroteaux type
StandardConditionSNOMED718559000Disorder
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 Acromesomelic dysplasia Maroteaux type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535661 | Acromesomelic dysplasia, Maroteaux type | Non-standard |
| Nebraska Lexicon | 718559000 | Acromesomelic dysplasia Maroteaux type | Non-standard |
Synonyms
Alternative names recorded for Acromesomelic dysplasia Maroteaux type across source vocabularies.
- Acromesomelic dysplasia Maroteaux type (disorder)
- displasia acromesomélica tipo Maroteaux
- displasia acromesomélica tipo Maroteaux (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(24)Roll up to these when you need a wider cohort.
- 1Acromesomelic dysplasia syndrome
- 1Autosomal recessive hereditary disorder
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 2Autosomal hereditary disorder
- 2Congenital anomaly of skeletal bone
- 2Developmental disorder
- 2Disorder of musculoskeletal system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Skeletal dysplasia
- 3Congenital anomaly of musculoskeletal system
- 3Disease
- 3Disorder of body system
- 3Disorder of bone development
- 3Disorder of skeletal system
- 3Genetic disease
- 3Musculoskeletal finding
- 4Clinical finding
- 4Congenital malformation
- 4Disorder of bone
- 5Bone finding
- 5Congenital disease
- 6Disorder of fetus and/or newborn
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