Search Ontology:
Human Disease

congenital disorder of glycosylation type IIl

Term ID
DOID:0070264
Synonyms
  • CDG IIl
  • CDG syndrome type IIL
  • CDG2L
  • CDGIIl
  • COG6-CGD
  • Congenital disorder of glycosylation type 2l
Definition
A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of the COG6 gene on chromosome 13q14.11. https://www.ncbi.nlm.nih.gov/pubmed/20605848
References
Ontology
Human Disease   ( DOID:0070264 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models