OMOP Concept 4281998
Cleidocranial dysostosis
StandardConditionSNOMED65976001Disorder
Maps from
5
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
5 source codes normalize to Cleidocranial dysostosis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 145059 | Cleidocranial Dysostosis | Non-standard |
| MeSH | D002973 | Cleidocranial Dysplasia | Non-standard |
| Nebraska Lexicon | 65976001 | Cleidocranial dysostosis | Non-standard |
| Read | PF5y000 | Cleidocranial dysostosis | Non-standard |
| Read | PF5y011 | Cleidocranial dysplasia | Non-standard |
Synonyms
Alternative names recorded for Cleidocranial dysostosis across source vocabularies.
- CCD - Cleidocranial dysplasia
- CLCD - Cleidocranial dysplasia
- Cleidocranial dysostosis (disorder)
- Cleidocranial dysplasia
- craneocleidodisostosis
- Craniocleidodysostosis
- disostosis cleidocraneal
- disostosis cleidocraneal (trastorno)
- displasia cleidocraneal
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(81)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Congenital anomaly of body wall
- 1Congenital anomaly of bone of shoulder girdle
- 1Congenital anomaly of thorax
- 1Congenital anomaly of tooth
- 1Developmental hereditary disorder
- 1Dysostosis of bone of skull
- 1Finding of clavicle structure
- 1Hereditary disorder of musculoskeletal system
- 1Hereditary disorder of tooth
- 2Autosomal hereditary disorder
- 2Congenital abnormality of oral cavity
- 2Congenital anomaly of digestive organ
- 2Congenital anomaly of jaw
- 2Congenital anomaly of skeletal bone
- 2Congenital anomaly of skull
- 2Congenital anomaly of upper limb
- 2Congenital anomaly of upper trunk
- 2Congenital malformation
- 2Developmental disorder
- 2Digestive system hereditary disorder
- 2Disorder of body wall
- 2Disorder of musculoskeletal system
- 2Disorder of shoulder
- 2Disorder of thorax
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