OBO ID: DOID:0070256
Term Name: congenital disorder of glycosylation type IId Search Ontology:
Synonyms:
  • CDG IId
  • CDG2D
  • CDGIId
Definition: A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of B4GALT1 on chromosome 9p21.1. https://www.ncbi.nlm.nih.gov/pubmed/11901181
References:
Ontology: Human Disease   (DOID:0070256)
OTHER congenital disorder of glycosylation type IId PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
B4GALT1 Congenital disorder of glycosylation, type IId 607091
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None