OMOP Concept 4080273
Combined malformation of central nervous system and skeletal muscle
StandardConditionSNOMED277949001Disorder
Maps from
1
Descendants
7
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Combined malformation of central nervous system and skeletal muscle via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 277949001 | Combined malformation of central nervous system and skeletal muscle | Non-standard |
Synonyms
Alternative names recorded for Combined malformation of central nervous system and skeletal muscle across source vocabularies.
- Combined malformation of central nervous system and skeletal muscle (disorder)
- malformación combinada del sistema nervioso central y músculo
- malformación combinada del sistema nervioso central y músculo (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(22)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of central nervous system
- 1Congenital anomaly of skeletal muscle
- 2Congenital anomaly of muscle AND/OR tendon
- 2Congenital anomaly of nervous system
- 2Disorder of skeletal muscle
- 2Disorder of the central nervous system
- 3Central nervous system finding
- 3Congenital anomaly of musculoskeletal system
- 3Congenital malformation
- 3Disorder of muscle
- 3Disorder of musculoskeletal system
- 3Disorder of nervous system
- 3Disorder of soft tissue
- 4Clinical finding
- 4Congenital disease
- 4Developmental disorder
- 4Disease
- 4Disorder of body system
- 4General finding of soft tissue
- 4Muscle finding
- 4Musculoskeletal finding
- 5Disorder of fetus and/or newborn
Narrower concepts
(7)Included automatically when you query with descendants.
- 1Congenital muscular dystrophy with cerebellar involvement
- 1Lethal hydranencephaly, diaphragmatic hernia syndrome
- 1Muscle eye brain disease
- 1Muscle-eye-brain disease, congenital muscular dystrophy
- 1Muscle eye brain disease with bilateral multicystic leukodystrophy
- 1Ophthalmoplegia, intellectual disability, lingua scrotalis syndrome
- 1Walker-Warburg congenital muscular dystrophy
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