OMOP Concept 4178826
Hereditary disorder of musculoskeletal system
StandardConditionSNOMED363212003Disorder
Maps from
4
Descendants
989
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
4 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 |
| ICD9CM | 359.21 | Myotonic muscular dystrophy | Non-standard |
| Nebraska Lexicon | 363212003 | Hereditary disorder of musculoskeletal system | 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
(989)Included automatically when you query with descendants.
- 13-M syndrome
- 146,XX disorder of sex development with skeletal anomalies syndrome
- 18q13 microdeletion syndrome
- 18q24.3 microdeletion syndrome
- 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
- 1Acropectorovertebral dysplasia
- 1Acrorenal mandibular syndrome
- 1Acrorenoocular syndrome
- 1Actin accumulation myopathy
- 1Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
- 1Adult-onset multiple mitochondrial deoxyribonucleic acid deletion syndrome due to deoxyguanosine kinase deficiency
- 1Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome
- 1Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome
- 1Agnathia, holoprosencephaly, situs inversus syndrome
- 1Allan-Herndon-Dudley syndrome
- 1Alpha-B crystallin-related late-onset myopathy
- 1Amish nemaline myopathy
- 1Amyotonia congenita
- 1Andersen Tawil syndrome
- 1Aneurysm osteoarthritis syndrome
- 1Angel-shaped phalangoepiphyseal dysplasia
- 1Aniridia and absent patella syndrome
- 1Ankylosing vertebral hyperostosis with tylosis syndrome
- 1Anterior maxillary protrusion, strabismus, intellectual disability syndrome
- 1Antley-Bixler syndrome
- 1Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome
- 1Aspartylglucosaminuria
- 1Asymmetric crying facies syndrome
- 1Atelosteogenesis
- 1Auriculo-condylar syndrome
- 1Autoimmune interstitial lung disease, arthritis syndrome
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