OMOP Concept 36713446

COG7 congenital disorder of glycosylation

StandardConditionSNOMED717773005Disorder
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 COG7 congenital disorder of glycosylation via the OMOP "Maps to" relationship.

Synonyms

Alternative names recorded for COG7 congenital disorder of glycosylation across source vocabularies.

  • Carbohydrate deficient glycoprotein syndrome type IIe
  • COG7 (component of oligomeric golgi complex 7) congenital disorder of glycosylation
  • Component of oligomeric golgi complex 7 congenital disorder of glycosylation
  • Component of oligomeric golgi complex 7 congenital disorder of glycosylation (disorder)
  • Congenital disorder of glycosylation type 2e
  • Congenital disorder of glycosylation type IIe
  • trastorno congénito de la glicosilación por alteración de COG7
  • trastorno congénito de la glicosilación por alteración de la subunidad 7 del complejo oligomérico del aparato de Golgi
  • trastorno congénito de la glicosilación por alteración de la subunidad 7 del complejo oligomérico del aparato de Golgi (trastorno)

Where it sits in the hierarchy

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

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