OMOP Concept 619007
Alpha-N-acetylgalactosaminidase deficiency type 2
StandardConditionSNOMED880065001Disorder
Maps from
0
Descendants
0
Valid from
31 Jan 2021
Valid to
31 Dec 2099
OMOP concepts
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Synonyms
Alternative names recorded for Alpha-N-acetylgalactosaminidase deficiency type 2 across source vocabularies.
- Alpha-N-acetylgalactosaminidase deficiency type 2 (disorder)
- deficiencia de Alfa-N-acetil galactosaminidasa tipo 2
- deficiencia de Alfa-N-acetil galactosaminidasa tipo 2 (trastorno)
- deficiencia de NAGA (alfa-N-acetilgalactosaminidasa) tipo 2
- enfermedad de Schindler tipo 2
- NAGA (alpha-N-acetylgalactosaminidase) deficiency type 2
- Schindler disease type 2
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(23)Roll up to these when you need a wider cohort.
- 1Alpha-N-acetylgalactosaminidase deficiency
- 2Autosomal recessive hereditary disorder
- 2Inherited metabolic disorder of nervous system
- 2Oligosaccharidosis
- 3Autosomal hereditary disorder
- 3Disorder of glycoprotein metabolism
- 3Disorder of lysosomal enzyme
- 3Hereditary disorder of nervous system
- 3Inborn error of metabolism
- 3Lysosomal storage disease
- 4Congenital disease
- 4Disorder of nervous system
- 4Enzymopathy
- 4Hereditary disease
- 4Hereditary disorder by system
- 4Hereditary metabolic disease
- 4Storage disease
- 5Disorder of body system
- 5Disorder of fetus and/or newborn
- 5Genetic disease
- 5Metabolic disease
- 6Disease
- 7Clinical finding
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