OMOP Concept 45773358
Allan-Herndon-Dudley syndrome
StandardConditionSNOMED702327009Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2014
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Allan-Herndon-Dudley syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537047 | Allan-Herndon-Dudley syndrome | Non-standard |
Synonyms
Alternative names recorded for Allan-Herndon-Dudley syndrome across source vocabularies.
- Allan-Herndon syndrome
- deficiencia de transportador 8 de monocarboxilato
- deficiencia de transportador 8 de monocarboxilato (trastorno)
- Monocarboxylate transporter 8 deficiency
- Monocarboxylate transporter 8 deficiency (disorder)
- síndrome de Allan-Herndon
- síndrome de Allan-Herndon-Dudley
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(81)Roll up to these when you need a wider cohort.
- 1Abnormal nervous system function
- 1Chronic disease of musculoskeletal system
- 1Decreased muscle tone
- 1Developmental hereditary disorder
- 1Disorder of skeletal muscle
- 1Genetic intellectual disability
- 1Hereditary disorder of musculoskeletal system
- 1Poor muscle tone
- 1Thyroid hormone responsiveness defect
- 1X-linked hereditary spastic paraplegia
- 1X-linked recessive hereditary disease
- 2Chronic disease
- 2Congenital disease
- 2Developmental disorder
- 2Disorder of muscle
- 2Disorder of musculoskeletal system
- 2Disorder of soft tissue
- 2Disorder of thyroid gland
- 2Finding of muscle tone
- 2Functional finding
- 2General finding of soft tissue
- 2Genetic disease
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Hereditary disorder of endocrine system
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