OMOP Concept 37118676
Congenital disorder of glycosylation type 1s
StandardConditionSNOMED733451007Disorder
Maps from
0
Descendants
0
Valid from
31 Jul 2017
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Congenital disorder of glycosylation type 1s across source vocabularies.
- ALG13-CDG (congenital disorder of glycosylation)
- Congenital disorder of glycosylation type 1s (disorder)
- Congenital disorder of glycosylation type Is
- trastorno congénito de glicosilación tipo 1s
- trastorno congénito de glicosilación tipo 1s (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(15)Roll up to these when you need a wider cohort.
- 1Carbohydrate-deficient glycoprotein syndrome type I
- 1X-linked recessive hereditary disease
- 2Carbohydrate-deficient glycoprotein syndrome
- 2X-linked hereditary disease
- 3Disorder of glycoprotein metabolism
- 3Sex-linked hereditary disorder
- 4Hereditary disease
- 4Inborn error of metabolism
- 5Congenital disease
- 5Genetic disease
- 5Hereditary metabolic disease
- 6Disease
- 6Fetal and/or neonatal disorder
- 6Metabolic disease
- 7Clinical finding
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