OMOP Concept 4178826
Hereditary disorder of musculoskeletal system
StandardConditionSNOMED363212003Disorder
Maps from
2
Descendants
1,004
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Hereditary disorder of musculoskeletal system via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 117581 | Inherited muscle weakness | Non-standard |
| ICD10CM | G71.20 | Congenital myopathy, unspecified | Non-standard |
Synonyms
Alternative names recorded for Hereditary disorder of musculoskeletal system across source vocabularies.
- Hereditary disorder of musculoskeletal system (disorder)
- trastorno hereditario del sistema musculoesquelético
- trastorno hereditario del sistema musculoesquelético (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(8)Roll up to these when you need a wider cohort.
Narrower concepts
(1,004)Included automatically when you query with descendants.
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- 1Absent radius, anogenital anomalies syndrome
- 1Absent thumb with short stature and immunodeficiency syndrome
- 1Absent tibia, polydactyly, arachnoid cyst syndrome
- 1Achondroplasia
- 1Acrocapitofemoral dysplasia
- 1Acrocephalopolysyndactyly type II
- 1Acrocephalosyndactyly type I
- 1Acrocephalosyndactyly type V
- 1Acrocraniofacial dysostosis
- 1Acrodysostosis
- 1Acrofacial dysostosis Catania type
- 1Acrofacial dysostosis Kennedy Teebi type
- 1Acrofacial dysostosis Palagonia type
- 1Acrofacial dysostosis Rodriguez type
- 1Acrofrontofacionasal dysostosis
- 1Acrofrontofacionasal dysostosis type 2
- 1Acromesomelic dysplasia Hunter-Thompson type
- 1Acromesomelic dysplasia Maroteaux type
- 1Acromicric dysplasia
- 1Acropectoral syndrome
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