OMOP Concept 37111243
Autosomal dominant myoglobinuria
StandardConditionSNOMED725903003Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Autosomal dominant myoglobinuria via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C563546 | Myoglobinuria, Autosomal Dominant | Non-standard |
Synonyms
Alternative names recorded for Autosomal dominant myoglobinuria across source vocabularies.
- Autosomal dominant myoglobinuria (disorder)
- mioglobinuria autosómica dominante
- mioglobinuria autosómica dominante (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(38)Roll up to these when you need a wider cohort.
- 1Abnormal urinary product
- 1Autosomal dominant hereditary disorder
- 1Lipid storage myopathy
- 1Myoglobinuria
- 2Autosomal hereditary disorder
- 2Detected by measurement
- 2Finding of urine substance level
- 2Hereditary disorder of musculoskeletal system
- 2Lipid storage disease
- 2Metabolic myopathy
- 2Protein level - finding
- 2Urine finding
- 3Clinical finding
- 3Disorder of lipid storage and metabolism
- 3Disorder of lysosomal enzyme
- 3Disorder of musculoskeletal system
- 3Disorder of skeletal muscle
- 3Finding of substance level
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Inborn error of metabolism
- 3Measurement finding
- 4Congenital disease
- 4Disorder of body system
- 4Disorder of lipoprotein AND/OR lipid metabolism
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