OMOP Concept 442180
Congenital anomaly of muscle AND/OR tendon
StandardConditionSNOMED79191007Disorder
Maps from
5
Descendants
209
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
5 source codes normalize to Congenital anomaly of muscle AND/OR tendon via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 144214 | Congenital Anomaly of Muscle and/or Tendon | Non-standard |
| ICD10CM | G71.29 | Other congenital myopathy | Non-standard |
| Nebraska Lexicon | 79191007 | Congenital malformation of muscles and tendons | Non-standard |
| Read | PGz0.00 | Unspecified anomaly of muscle | Non-standard |
| Read | PGz1.00 | Unspecified anomaly of tendon | Non-standard |
Synonyms
Alternative names recorded for Congenital anomaly of muscle AND/OR tendon across source vocabularies.
- anomalía congénita de músculo Y/O tendón
- anomalía congénita de músculo Y/O tendón (trastorno)
- anomalía congénita de músculo y tendón
- Congenital anomaly of muscle AND/OR tendon (disorder)
- Congenital malformation of muscles and tendons
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(10)Roll up to these when you need a wider cohort.
Narrower concepts
(209)Included automatically when you query with descendants.
- 1Congenital absence of muscle AND/OR tendon
- 1Congenital anomaly of skeletal muscle
- 1Congenital shortening of tendon
- 1Congenital trigger finger of left hand
- 1Congenital trigger finger of right hand
- 1Extensor tendons of finger anomalies
- 2Aberrant muscle of the lower limb
- 2Aberrant muscle of the upper limb
- 2Accessory skeletal muscle
- 2Amyotrophia congenita
- 2Asymmetric crying facies syndrome
- 2Benign congenital myopathy
- 2Central core disease
- 2Combined malformation of central nervous system and skeletal muscle
- 2Congenital absence of skeletal muscle
- 2Congenital absence of tendon
- 2Congenital anomaly of diaphragm
- 2Congenital anomaly of sternocleidomastoid muscle
- 2Congenital contracture of gastrocnemius muscle
- 2Congenital fibrosis syndrome
- 2Congenital hereditary muscular dystrophy
- 2Congenital lethal myopathy Compton North type
- 2Congenital myopathy with abnormal subcellular organelles
- 2Congenital myopathy with internal nuclei and atypical cores
- 2Congenital myopathy with myasthenic-like onset
- 2Congenital nonprogressive myopathy with Moebius and Robin sequences
- 2Congenital short Achilles tendon
- 2Congenital short quadriceps
- 2Congenital trigger finger of bilateral hands
- 2Cylindrical spirals myopathy
- 2Duane anomaly, myopathy, scoliosis syndrome
- 2Early-onset myopathy, areflexia, respiratory distress, dysphagia syndrome
- 2Floppy infant syndrome
- 2Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome
- 2Hypoplasia of eye muscle
- 2Intellectual disability, developmental delay, contracture syndrome
- 2Intellectual disability, myopathy, short stature, endocrine defect syndrome
- 2Isolated asymmetric crying facies
- 2King Denborough syndrome
- 2Klippel-Feil anomaly, myopathy, facial dysmorphism syndrome
- 2Lethal congenital contracture syndrome type 2
- 2Lethal congenital contracture syndrome type 5
- 2Lethal multiple pterygium syndrome
- 2Malignant hyperthermia with arthrogryposis and torticollis syndrome
- 2Multi-core congenital myopathy
- 2Myopathic Ehlers-Danlos syndrome
- 2Myopathy with abnormality of histochemical fiber type
- 2Myopathy with cytoplasmic inclusions
- 2Myotubular myopathy
- 2Native American myopathy
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