OMOP Concept 4025195
Osteochondrodysplasia syndrome
StandardConditionSNOMED105985007Disorder
Maps from
1
Descendants
53
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Osteochondrodysplasia syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | D010009 | Osteochondrodysplasias | Non-standard |
Synonyms
Alternative names recorded for Osteochondrodysplasia syndrome across source vocabularies.
- Osteochondrodysplasia syndrome (disorder)
- síndrome de osteocondrodisplasia
- síndrome de osteocondrodisplasia (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(8)Roll up to these when you need a wider cohort.
Narrower concepts
(53)Included automatically when you query with descendants.
- 1Atelosteogenesis
- 1Chondroectodermal dysplasia
- 1Complex lethal osteochondrodysplasia
- 1Craniometaphyseal dysplasia
- 1Dysplasias with significant membranous bone involvement
- 1Frontometaphyseal dysplasia
- 1Hajdu-Cheney syndrome
- 1Kenny syndrome
- 1Kniest dysplasia
- 1Kniest-Stickler dysplasia
- 1Lethal Kniest-like syndrome
- 1Metaphyseal chondrodysplasia, Jansen type
- 1Metatropic dysplasia
- 1Osteodysplastic primordial dwarfism
- 1Otospondylomegaepiphyseal dysplasia
- 1Spondylocarpotarsal synostosis syndrome
- 1Spondyloepimetaphyseal dysplasia, Strudwick type
- 1Spondyloepiphyseal dysplasia tarda
- 1Spondyloperipheral dysplasia
- 1Thanatophoric dysplasia
- 2Atelosteogenesis type 1
- 2Atelosteogenesis type 2
- 2Atelosteogenesis type 3
- 2Chondroectodermal dysplasia with night blindness syndrome
- 2Craniometaphyseal dysplasia - mild type
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