OMOP Concept 36715329
Fibular aplasia and ectrodactyly syndrome
StandardConditionSNOMED720952001Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Fibular aplasia and ectrodactyly syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 720952001 | Aplasia of fibula and ectrodactyly syndrome | Non-standard |
Synonyms
Alternative names recorded for Fibular aplasia and ectrodactyly syndrome across source vocabularies.
- Aplasia of fibula and ectrodactyly syndrome
- Aplasia of fibula and ectrodactyly syndrome (disorder)
- Familial ectrodactyly with fibular aplasia
- síndrome de aplasia de peroné y ectrodactilia
- síndrome de aplasia de peroné y ectrodactilia (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(52)Roll up to these when you need a wider cohort.
- 1Aplasia of fibula
- 1Autosomal dominant hereditary disorder
- 1Developmental hereditary disorder
- 1Dysostosis
- 1Ectrodactyly
- 1Hereditary disorder of musculoskeletal system
- 1Multiple malformation syndrome with limb defect as major feature
- 2Adactyly
- 2Aplasia of bone of lower limb
- 2Autosomal hereditary disorder
- 2Congenital absence of fibula
- 2Congenital anomaly of skeletal bone
- 2Developmental disorder
- 2Disorder of musculoskeletal system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Multiple system malformation syndrome
- 2Skeletal dysplasia
- 3Absence of fibula
- 3Absence of lower limb
- 3Aplasia of bone structure of extremity
- 3Congenital absence of skeletal bone
- 3Congenital anomaly of digit
- 3Congenital anomaly of fibula
- 3Congenital anomaly of lower limb
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