COG5 congenital disorder of glycosylation

Source codes that map to this concept

1 source code normalizes to COG5 congenital disorder of glycosylation via the OMOP "Maps to" relationship.

Synonyms

Alternative names recorded for COG5 congenital disorder of glycosylation across source vocabularies.

• Carbohydrate deficient glycoprotein syndrome type IIi
• CDG2I - carbohydrate deficient glycoprotein syndrome type IIi
• COG5 (component of oligomeric golgi complex 5) congenital disorder of glycosylation
• Component of oligomeric golgi complex 5 congenital disorder of glycosylation
• Component of oligomeric golgi complex 5 congenital disorder of glycosylation (disorder)
• Congenital disorder of glycosylation type IIi
• trastorno congénito de la glicosilación por alteración de COG5
• trastorno congénito de la glicosilación por alteración de la subunidad 5 del complejo oligomérico del aparato de Golgi
• trastorno congénito de la glicosilación por alteración de la subunidad 5 del complejo oligomérico del aparato de Golgi (trastorno)

Where it sits in the hierarchy

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

Get this concept via the API

Resolve COG5 congenital disorder of glycosylation - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.

curl "https://api.omophub.com/v1/concepts/36715426?include_relationships=true" \
  -H "Authorization: Bearer $OMOPHUB_API_KEY"