OMOP Concept 4133493
Craniometadiaphyseal dysplasia
StandardConditionSNOMED278833002Disorder
Maps from
2
Descendants
1
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Craniometadiaphyseal dysplasia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537519 | Schwartz-Lelek syndrome | Non-standard |
| Nebraska Lexicon | 278833002 | Craniometadiaphyseal dysplasia | Non-standard |
Synonyms
Alternative names recorded for Craniometadiaphyseal dysplasia across source vocabularies.
- Craniometadiaphyseal dysplasia (disorder)
- displasia craneometadiafisiaria
- displasia craneometadiafisiaria (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(35)Roll up to these when you need a wider cohort.
- 1Dysplasia with increased bone density
- 1Osteochondrodysplasia with osteopetrosis
- 2Bone density above reference range
- 2Disorder of bone
- 2Osteopetrosis
- 2Skeletal dysplasia
- 3Bone densimetry abnormal
- 3Bone density finding
- 3Bone finding
- 3Chronic disease of musculoskeletal system
- 3Congenital anomaly of musculoskeletal system
- 3Congenital anomaly of skeletal bone
- 3Developmental hereditary disorder
- 3Disorder of skeletal system
- 3Hereditary disorder of musculoskeletal system
- 3Measurement finding above reference range
- 4Chronic disease
- 4Congenital malformation
- 4Developmental disorder
- 4Disorder of bone development
- 4Disorder of musculoskeletal system
- 4Hereditary disease
- 4Hereditary disorder by system
- 4Imaging finding
- 4Measurement finding outside reference range
Narrower concepts
(1)Included automatically when you query with descendants.
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