OMOP Concept 36714254
Mesomelic dysplasia Kantaputra type
StandardConditionSNOMED719397009Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Mesomelic dysplasia Kantaputra type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535547 | Kantaputra Gorlin syndrome | Non-standard |
Synonyms
Alternative names recorded for Mesomelic dysplasia Kantaputra type across source vocabularies.
- displasia mesomélica tipo Kantaputra
- displasia mesomélica tipo Kantaputra (trastorno)
- Kantaputra mesomelic dysplasia
- Mesomelic dysplasia Kantaputra type (disorder)
- Mesomelic dysplasia Thai type
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(72)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Bowing of upper limb
- 1Congenital abnormal shape of humerus
- 1Congenital abnormal shape of radius
- 1Congenital anomalies of elbow and upper arm
- 1Congenital bowing of long bone
- 1Congenital deformity of bone of forearm
- 1Deformity of radius
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 1Mesomelic dysplasia
- 1Multiple malformation syndrome with limb defect as major feature
- 1Short stature disorder
- 2Autosomal hereditary disorder
- 2Bowing deformity of bone
- 2Congenital anomaly of humerus
- 2Congenital anomaly of radius
- 2Congenital anomaly of skeletal bone
- 2Congenital anomaly of upper limb
- 2Congenital deformity of musculoskeletal system
- 2Congenital deformity of upper limb
- 2Congenital dysplasia of limb
- 2Congenital malformation syndrome
- 2Deformation of bone
- 2Deformity of upper limb
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