OMOP Concept 4079882
Loss of single peroxisomal function
StandardConditionSNOMED238066006Disorder
Maps from
1
Descendants
17
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Loss of single peroxisomal function via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 238066006 | Loss of single peroxisomal function | Non-standard |
Synonyms
Alternative names recorded for Loss of single peroxisomal function across source vocabularies.
- Loss of single peroxisomal function (disorder)
- pérdida de una función aislada de los peroxisomas
- pérdida de una función aislada de los peroxisomas (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(10)Roll up to these when you need a wider cohort.
Narrower concepts
(17)Included automatically when you query with descendants.
- 1Acatalasemia
- 1Acyl-CoA oxidase deficiency
- 1Adrenoleukodystrophy
- 1Bifunctional peroxisomal enzyme deficiency
- 1Contiguous ABCD1 DXS1357E deletion syndrome
- 1Dihydroxycholestanoic acidemia and trihydroxycholestanoic acidemia
- 1Fatty acyl-CoA reductase 1 deficiency
- 1Glutaryl-CoA oxidase deficiency
- 1Isolated alkyldihydroxyacetone phosphate synthase deficiency
- 1Isolated dihydroxyacetone phosphate acyltransferase deficiency
- 1Leukoencephalopathy, dystonia, motor neuropathy syndrome
- 1Peroxisomal thiolase deficiency
- 1Primary hyperoxaluria, type I
- 2Adolescent X-linked adrenoleukodystrophy
- 2Adrenomyeloneuropathy
- 2Childhood cerebral X-linked adrenoleukodystrophy
- 2Neonatal adrenoleukodystrophy
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