OMOP Concept 36715112
Campomelia Cumming type
StandardConditionSNOMED720599002Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Campomelia Cumming type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537966 | Campomelia Cumming type | Non-standard |
| Nebraska Lexicon | 720599002 | Campomelia Cumming type | Non-standard |
Synonyms
Alternative names recorded for Campomelia Cumming type across source vocabularies.
- Campomelia Cumming type (disorder)
- campomelia tipo Cumming
- campomelia tipo Cumming (trastorno)
- Cumming syndrome
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(38)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Bent bone dysplasia group
- 1Congenital anomaly of limb
- 1Congenital deformity of musculoskeletal system
- 1Deformation of bone
- 1Deformity of limb
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 1Lymphedema
- 1Multiple malformation syndrome with limb defect as major feature
- 2Autosomal hereditary disorder
- 2Bone finding
- 2Congenital anomaly of musculoskeletal system
- 2Congenital anomaly of skeletal bone
- 2Congenital deformity
- 2Congenital malformation
- 2Deformity
- 2Developmental disorder
- 2Disorder characterized by edema
- 2Disorder of limb
- 2Disorder of musculoskeletal system
- 2Finding of limb structure
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Multiple system malformation syndrome
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