OMOP Concept 36715313
Encephalopathy due to prosaposin deficiency
StandardConditionSNOMED720864008Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Encephalopathy due to prosaposin deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 720864008 | Encephalopathy due to prosaposin deficiency | Non-standard |
Synonyms
Alternative names recorded for Encephalopathy due to prosaposin deficiency across source vocabularies.
- Combined prosaposin deficiency
- Combined saposin deficiency
- deficiencia combinada de prosaposina
- encefalopatía debida a deficiencia de prosaposina
- encefalopatía debida a deficiencia de prosaposina (trastorno)
- Encephalopathy due to prosaposin deficiency (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(28)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Disorder of brain
- 1Inherited metabolic disorder of nervous system
- 1Sphingolipidosis
- 2Autosomal hereditary disorder
- 2Disorder of head
- 2Disorder of lipid storage and metabolism
- 2Disorder of the central nervous system
- 2Finding of brain
- 2Hereditary disorder of nervous system
- 2Inborn error of metabolism
- 2Lysosomal storage disease
- 3Central nervous system finding
- 3Congenital disease
- 3Disease
- 3Disorder of lipoprotein AND/OR lipid metabolism
- 3Disorder of nervous system
- 3Enzymopathy
- 3Head finding
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Hereditary metabolic disease
- 3Storage disease
- 4Clinical finding
- 4Disorder of body system
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