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Human Disease and Mouse Model Detail
Human Disease Congenital Disorder of Glycosylation, Type IB; CDG1B
OMIM ID: 602579
Human Phenotype Ontology associations
Synonyms Cdg IB; CDGIB; CDG, Gastrointestinal Type; Congenital Disorders of Glycosylation, Type I; Mannosephosphate Isomerase Deficiency; MPI Deficiency; Protein-Losing Enteropathy-Hepatic Fibrosis Syndrome; Saguenay-Lac Saint-Jean Syndrome; SLSJ SYNDROME
View all models View ALL (1) "NOT" mouse models for this human disease. No mouse models with similarity to the expected human disease phenotype are reported in MGI.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     MPI* Mpi View 1 "NOT" model HomoloGene and HGNC

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory