OMOP Concept 37165108
Fatty acyl-CoA reductase 1 deficiency
StandardConditionSNOMED1237619001Disorder
Maps from
0
Descendants
0
Valid from
30 Sept 2022
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Fatty acyl-CoA reductase 1 deficiency across source vocabularies.
- deficiencia de Acil-CoA reductasa 1 de ácidos grasos
- deficiencia de Acil-coenzima A reductasa 1 de ácidos grasos
- deficiencia de Acil-coenzima A reductasa 1 de ácidos grasos (trastorno)
- deficiencia de gen FAR1
- FAR1 deficiency
- Fatty acyl-coenzyme A reductase 1 deficiency
- Fatty acyl-coenzyme A reductase 1 deficiency (disorder)
- PFCRD - peroxisomal fatty acyl-CoA reductase 1 disorder
- trastorno de acil-CoA reductasa 1 de ácidos grasos peroxisomal
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(61)Roll up to these when you need a wider cohort.
- 1Abnormal nervous system function
- 1Autosomal recessive hereditary disorder
- 1Developmental hereditary disorder
- 1Epilepsy
- 1Genetic intellectual disability
- 1Global developmental delay
- 1Inherited metabolic disorder of nervous system
- 1Loss of single peroxisomal function
- 1Microcephaly
- 1Multiple system malformation syndrome
- 1Neurodevelopmental delay
- 1Severe intellectual disability
- 1Short stature disorder
- 2Autosomal hereditary disorder
- 2Congenital malformation syndrome
- 2Developmental delay
- 2Developmental disorder
- 2Disorder of peroxisomal function
- 2Disorder of stature
- 2Finding of head circumference
- 2Functional finding
- 2Genetic disease
- 2Hereditary disease
- 2Hereditary disorder of nervous system
- 2Inborn error of metabolism
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