OMOP Concept 4160748
Chondrodysplasia punctata, Conradi-Hünermann type
StandardConditionSNOMED398719004Disorder
Maps from
4
Descendants
0
Valid from
31 Jul 2003
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
4 source codes normalize to Chondrodysplasia punctata, Conradi-Hünermann type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 145564 | Chondrodysplasia punctata, Conradi-Hünermann type | Non-standard |
| Read | PG56000 | Chondrodysplasia calcificans congenita | Non-standard |
| Read | PG56011 | Chondrodysplasia calcificans congenita | Non-standard |
| Read | PG56012 | Conradi - Hunermann syndrome | Non-standard |
Synonyms
Alternative names recorded for Chondrodysplasia punctata, Conradi-Hünermann type across source vocabularies.
- Chondrodysplasia calcificans congenita
- Chondrodysplasia punctata, Conradi-Hunermann type
- Chondrodysplasia punctata, Conradi-Hünermann type (disorder)
- condrodisplasia punteada tipo Conradi-Hünermann
- condrodisplasia punteada tipo Conradi-Hünermann (trastorno)
- Conradi disease
- Conradi-Hunermann syndrome
- Conradi-Hünermann syndrome
- Conradi's syndrome
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(19)Roll up to these when you need a wider cohort.
- 1Chondrodysplasia punctata
- 2Congenital anomaly of skeletal bone
- 2Lesion of bone
- 2Skeletal dysplasia
- 3Congenital anomaly of musculoskeletal system
- 3Disorder of bone
- 3Disorder of bone development
- 3Structural abnormality of skeleton
- 4Bone finding
- 4Congenital malformation
- 4Developmental disorder
- 4Disorder of musculoskeletal system
- 4Disorder of skeletal system
- 5Congenital disease
- 5Disease
- 5Disorder of body system
- 5Musculoskeletal finding
- 6Clinical finding
- 6Fetal and/or neonatal disorder
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