OMOP Concept 36715348

ALG9 congenital disorder of glycosylation

StandardConditionSNOMED720978005Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept

2 source codes normalize to ALG9 congenital disorder of glycosylation via the OMOP "Maps to" relationship.

Synonyms

Alternative names recorded for ALG9 congenital disorder of glycosylation across source vocabularies.

  • ALG9-CDG - asparagine-linked glycosylation 9 congenital disorder of glycosylation
  • Asparagine-linked glycosylation 9 congenital disorder of glycosylation
  • Asparagine-linked glycosylation 9 congenital disorder of glycosylation (disorder)
  • Carbohydrate deficient glycoprotein syndrome type IL
  • Congenital disorder of glycosylation type 1L
  • Congenital disorder of glycosylation type IL
  • Mannosyltransferase 7-9 deficiency
  • trastorno congénito de glicosilación 9 vinculado a asparagina
  • trastorno congénito de glicosilación 9 vinculado a asparagina (trastorno)

Where it sits in the hierarchy

Ordered by distance - 1 is a direct parent or child.

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