OMOP Concept 4144975
Nievergelt's syndrome
StandardConditionSNOMED33979003Disorder
Maps from
3
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
3 source codes normalize to Nievergelt's syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 133029 | Nievergelt's syndrome | Non-standard |
| MeSH | C536120 | Nievergelt syndrome | Non-standard |
| Nebraska Lexicon | 33979003 | Nievergelt syndrome | Non-standard |
Synonyms
Alternative names recorded for Nievergelt's syndrome across source vocabularies.
- Mesomelic dysplasia - Nievergelt type
- Nievergelt-Erb syndrome
- Nievergelt's syndrome (disorder)
- Nievergelt syndrome
- síndrome de Nievergelt
- síndrome de Nievergelt - Erb
- síndrome de Nievergelt (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(42)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Congenital abnormal shape of fibula
- 1Congenital abnormal shape of tibia
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 1Mesomelic dysplasia
- 1Multiple malformation syndrome with limb defect as major feature
- 2Autosomal hereditary disorder
- 2Congenital anomaly of fibula
- 2Congenital anomaly of skeletal bone
- 2Congenital anomaly of tibia
- 2Congenital dysplasia of limb
- 2Congenital malformation syndrome
- 2Developmental disorder
- 2Disorder of musculoskeletal system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Multiple system malformation syndrome
- 2Skeletal dysplasia
- 3Congenital anomaly of limb
- 3Congenital anomaly of lower limb
- 3Congenital anomaly of musculoskeletal system
- 3Congenital malformation
- 3Disease
- 3Disorder of body system
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