OMOP Concept 37116408
Congenital disorder of glycosylation type 1w
StandardConditionSNOMED733111000Disorder
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 1w across source vocabularies.
- Congenital disorder of glycosylation type 1w (disorder)
- Congenital disorder of glycosylation type Iw
- STT3A-CDG (congenital disorder of glycosylation)
- trastorno congénito de glicosilación tipo 1w
- trastorno congénito de glicosilación tipo 1w (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(14)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Carbohydrate-deficient glycoprotein syndrome type I
- 2Autosomal hereditary disorder
- 2Carbohydrate-deficient glycoprotein syndrome
- 3Disorder of glycoprotein metabolism
- 3Hereditary disease
- 4Genetic disease
- 4Inborn error of metabolism
- 5Congenital disease
- 5Disease
- 5Hereditary metabolic disease
- 6Clinical finding
- 6Fetal and/or neonatal disorder
- 6Metabolic disease
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