OMOP Concept 4006933
Chondrodysplasia
StandardConditionSNOMED205465004Disorder
Maps from
7
Descendants
16
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
7 source codes normalize to Chondrodysplasia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 205465004 | Chondrodysplasia | Non-standard |
| OXMIS | 7564CD | CHONDRODYSPLASIA | Non-standard |
| Read | PG4..00 | Chondrodysplasia | Non-standard |
| Read | PG40.00 | Chondrodysplasia, unspecified | Non-standard |
| Read | PG42.13 | Chondrodysplasia | Non-standard |
| Read | PG42z00 | Dyschondroplasia NOS | Non-standard |
| Read | PG4y.00 | Chondrodysplasia OS | Non-standard |
Synonyms
Alternative names recorded for Chondrodysplasia across source vocabularies.
- Chondrodysplasia (disorder)
- condrodisplasia
- condrodisplasia (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(16)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of skeletal bone
- 1Skeletal dysplasia
- 2Congenital anomaly of musculoskeletal system
- 2Disorder of bone development
- 2Disorder of skeletal system
- 3Congenital malformation
- 3Developmental disorder
- 3Disorder of bone
- 3Disorder of musculoskeletal system
- 4Bone finding
- 4Congenital disease
- 4Disease
- 4Disorder of body system
- 4Musculoskeletal finding
- 5Clinical finding
- 5Disorder of fetus and/or newborn
Narrower concepts
(16)Included automatically when you query with descendants.
- 1Achondroplasia
- 1Bone dysplasia lethal Holmgren type
- 1Brachydactylous dwarfism Mseleni type
- 1Camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia syndrome
- 1Chondrodysplasia with disorder of sex development syndrome
- 1Chondrodysplasia with joint dislocations gPAPP type
- 1Fibrochondrogenesis
- 1Lethal chondrodysplasia with fragmented bone
- 1Lethal recessive chondrodysplasia
- 1Lethal retarded ossification syndromes
- 1QRICH1-related intellectual disability, chondrodysplasia syndrome
- 1X-linked dominant chondrodysplasia Chassaing Lacombe type
- 2Astley-Kendall dysplasia
- 2Dappled diaphyseal dysplasia
- 2Greenberg dysplasia
- 2Severe achondroplasia, developmental delay, acanthosis nigricans syndrome
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