OMOP Concept 4235431
Muscle AMP deaminase deficiency
StandardConditionSNOMED9105005Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Muscle AMP deaminase deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 133641 | Muscle Amp Deaminase Deficiency | Non-standard |
| ICD10CM | E79.2 | Myoadenylate deaminase deficiency | Non-standard |
Synonyms
Alternative names recorded for Muscle AMP deaminase deficiency across source vocabularies.
- deficiencia de AMP desaminasa muscular
- deficiencia de AMP desaminasa muscular (trastorno)
- deficiencia de la AMP deaminasa muscular
- deficiencia de la mioadenilato deaminasa
- deficiencia de mioadenilato desaminasa
- miopatía por deficiencia de mioadenilato deaminasa
- miopatía por deficiencia de mioadenilato desaminasa
- Muscle adenosine monophosphate deaminase deficiency
- Muscle adenosine monophosphate deaminase deficiency (disorder)
- Muscle adenylate deaminase deficiency
- Myoadenylate deaminase deficiency
- Myoadenylate deaminase deficiency myopathy
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(21)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Disorder of purine metabolism
- 1Enzymopathy
- 1Hereditary disorder of musculoskeletal system
- 1Metabolic myopathy
- 2Autosomal hereditary disorder
- 2Disorder of musculoskeletal system
- 2Disorder of purine and pyrimidine metabolism
- 2Disorder of skeletal muscle
- 2Hereditary disorder by system
- 2Metabolic disease
- 3Disease
- 3Disorder of body system
- 3Disorder of muscle
- 3Disorder of soft tissue
- 3Hereditary disease
- 3Musculoskeletal finding
- 4Clinical finding
- 4General finding of soft tissue
- 4Genetic disease
- 4Muscle finding
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