OMOP Concept 37110837
Mucolipidosis type IV
StandardConditionSNOMED725296006Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Mucolipidosis type IV via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 139648 | Ganglioside Sialidase Deficiency | Non-standard |
| ICD10CM | E75.11 | Mucolipidosis IV | Non-standard |
Synonyms
Alternative names recorded for Mucolipidosis type IV across source vocabularies.
- mucolipidosis tipo IV
- mucolipidosis tipo IV (trastorno)
- Mucolipidosis type IV (disorder)
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
- 1Inherited metabolic disorder of nervous system
- 1Mucolipidosis
- 2Autosomal hereditary disorder
- 2Disorder of lysosomal enzyme
- 2Hereditary disorder of nervous system
- 2Inborn error of metabolism
- 2Lysosomal storage disease
- 3Congenital disease
- 3Disorder of nervous system
- 3Enzymopathy
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Hereditary metabolic disease
- 3Storage disease
- 4Disorder of body system
- 4Fetal and/or neonatal disorder
- 4Genetic disease
- 4Metabolic disease
- 5Disease
- 6Clinical finding
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