OMOP Concept 4150458
Chondrodysplasia punctata
StandardConditionSNOMED278715001Disorder
Maps from
12
Descendants
13
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
12 source codes normalize to Chondrodysplasia punctata via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 145566 | Chondrodysplasia punctata | Non-standard |
| CIM10 | Q77.3 | Chondrodysplasia punctata | Non-standard |
| HPO | HP_0010655 | Epiphyseal stippling | Non-standard |
| ICD10 | Q77.3 | Chondrodysplasia punctata | Non-standard |
| ICD10CM | Q77.3 | Chondrodysplasia punctata | Non-standard |
| ICD10CN | Q77.3 | Chondrodysplasia punctata | Non-standard |
| ICD10CN | Q77.300 | Chondrodysplasia punctata | Non-standard |
| ICD10CN | Q77.301 | Congenital multiple epiphyseal dysplasia (machine translation) | Non-standard |
| ICD10GM | Q77.3 | Chondrodysplasia punctata | Non-standard |
| KCD7 | Q77.3 | Chondrodysplasia punctata | Non-standard |
| MeSH | D002806 | Chondrodysplasia Punctata | Non-standard |
| Read | PG4C.00 | Chondrodysplasia punctata | Non-standard |
Synonyms
Alternative names recorded for Chondrodysplasia punctata across source vocabularies.
- Chondrodysplasia punctata (stippled epiphyses) group
- Chondrodysplasia punctata (stippled epiphyses) group (disorder)
- condrodisplasia punctata
- grupo de la condrodisplasia punctata
- grupo de la condrodisplasia punctata (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(18)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of skeletal bone
- 1Lesion of bone
- 1Skeletal dysplasia
- 2Congenital anomaly of musculoskeletal system
- 2Disorder of bone
- 2Disorder of bone development
- 2Structural abnormality of skeleton
- 3Bone finding
- 3Congenital malformation
- 3Developmental disorder
- 3Disorder of musculoskeletal system
- 3Disorder of skeletal system
- 4Congenital disease
- 4Disease
- 4Disorder of body system
- 4Musculoskeletal finding
- 5Clinical finding
- 5Fetal and/or neonatal disorder
Narrower concepts
(13)Included automatically when you query with descendants.
- 1Brachytelephalangic chondrodysplasia punctata
- 1Chondrodysplasia punctata, Conradi-Hünermann type
- 1Chondrodysplasia punctata due to maternal autoimmune disease
- 1Chondrodysplasia punctata, MT type
- 1Chondrodysplasia punctata Toriello type
- 1Chondrodysplasia punctata, X-linked dominant type
- 1Chondrodysplasia punctata, X-linked recessive type
- 1Hyperphosphatasia-osteoectasia syndrome
- 1Lissencephaly type 3 metacarpal bone dysplasia syndrome
- 1Rhizomelic chondrodysplasia punctata syndrome
- 2Rhizomelic chondrodysplasia punctata type 1
- 2Rhizomelic chondrodysplasia punctata type 2
- 2Rhizomelic chondrodysplasia punctata type 3
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