OMOP Concept 4233941
Congenital anomaly of skeletal muscle
StandardConditionSNOMED89886004Disorder
Maps from
9
Descendants
217
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
9 source codes normalize to Congenital anomaly of skeletal muscle via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 120053 | Congenital Anomaly of Skeletal Muscle | Non-standard |
| CIM10 | G71.2 | Congenital myopathies | Non-standard |
| ICD10 | G71.2 | Congenital myopathies | Non-standard |
| ICD10CM | G71.2 | Congenital myopathies | Non-standard |
| ICD10CN | G71.2 | Congenital myopathies | Non-standard |
| ICD10CN | G71.200 | Congenital myopathies | Non-standard |
| ICD10GM | G71.2 | Congenital myopathies | Non-standard |
| KCD7 | G71.2 | Congenital myopathies | Non-standard |
| Read | F390500 | Congenital myopathy | Non-standard |
Synonyms
Alternative names recorded for Congenital anomaly of skeletal muscle across source vocabularies.
- anomalía congénita del músculo esquelético
- anomalía congénita del músculo esquelético (trastorno)
- Congenital anomaly of skeletal muscle (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(16)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of muscle AND/OR tendon
- 1Disorder of skeletal muscle
- 2Congenital anomaly of musculoskeletal system
- 2Disorder of muscle
- 2Disorder of musculoskeletal system
- 2Disorder of soft tissue
- 3Congenital malformation
- 3Disease
- 3Disorder of body system
- 3General finding of soft tissue
- 3Muscle finding
- 3Musculoskeletal finding
- 4Clinical finding
- 4Congenital disease
- 4Developmental disorder
- 5Fetal and/or neonatal disorder
Narrower concepts
(217)Included automatically when you query with descendants.
- 1Aberrant muscle of the lower limb
- 1Aberrant muscle of the upper limb
- 1Accessory skeletal muscle
- 1Amyotrophia congenita
- 1Asymmetric crying facies syndrome
- 1Benign congenital myopathy
- 1Central core disease
- 1Combined malformation of central nervous system and skeletal muscle
- 1Congenital absence of skeletal muscle
- 1Congenital anomaly of diaphragm
- 1Congenital anomaly of sternocleidomastoid muscle
- 1Congenital contracture of gastrocnemius muscle
- 1Congenital fibrosis syndrome
- 1Congenital hereditary muscular dystrophy
- 1Congenital hypoplasia of muscle of abdominal wall
- 1Congenital hypoplasia of muscle of limb
- 1Congenital hypoplasia of muscle of neck
- 1Congenital hypoplasia of muscle of pelvis
- 1Congenital hypoplasia of pectoral muscle
- 1Congenital lethal myopathy Compton North type
- 1Congenital myopathy with abnormal subcellular organelles
- 1Congenital myopathy with internal nuclei and atypical cores
- 1Congenital myopathy with myasthenic-like onset
- 1Congenital nonprogressive myopathy with Moebius and Robin sequences
- 1Cylindrical spirals myopathy
Showing 25 of 217. Retrieve the full set via the API.
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