OMOP Concept 4006936
Mesomelic dysplasia
StandardConditionSNOMED205473008Disorder
Maps from
2
Descendants
18
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Mesomelic dysplasia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| HPO | HP_0003027 | Mesomelia | Non-standard |
| Read | PG44300 | Mesomelic dysplasia | Non-standard |
Synonyms
Alternative names recorded for Mesomelic dysplasia across source vocabularies.
- displasia mesomélica
- displasia mesomélica (trastorno)
- Mesomelic dysplasia (disorder)
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.
- 1Congenital anomaly of skeletal bone
- 1Congenital dysplasia of limb
- 1Congenital malformation syndrome
- 1Lesion of bone
- 1Skeletal dysplasia
- 1Structural abnormality of bone of limb
- 2Congenital anomaly of limb
- 2Congenital anomaly of musculoskeletal system
- 2Congenital malformation
- 2Disorder of bone
- 2Disorder of bone development
- 2Disorder of limb
- 2Structural abnormality of skeleton
- 3Bone finding
- 3Congenital disease
- 3Developmental disorder
- 3Disease
- 3Disorder of musculoskeletal system
- 3Disorder of skeletal system
- 3Finding of limb structure
- 4Clinical finding
- 4Disorder of body system
- 4Fetal and/or neonatal disorder
- 4Musculoskeletal finding
Narrower concepts
(18)Included automatically when you query with descendants.
- 1Brachydactyly type A6
- 1Congenital hypoplasia of ulna and intellectual disability syndrome
- 1Langer mesomelic dysplasia syndrome
- 1Leri-Weill dyschondrosteosis
- 1Mesomelic dysplasia, digital anomalies, intellectual disability syndrome
- 1Mesomelic dysplasia Kantaputra type
- 1Mesomelic dysplasia of lower limb
- 1Mesomelic dysplasia of upper limb
- 1Nievergelt's syndrome
- 1Reardon Hall Slaney syndrome
- 1Reinhardt Pfeiffer mesomelic dysplasia
- 1Robinow syndrome
- 1X-linked spondyloepimetaphyseal dysplasia
- 2Autosomal dominant Robinow syndrome
- 2Autosomal recessive Robinow syndrome
- 2Brachydactyly, mesomelia, intellectual disability, heart defect syndrome
- 2EN1-related dorsoventral syndrome
- 2Mesomelic dysplasia Savarirayan type
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