About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease Congenital Disorder of Glycosylation, Type It; CDG1T
OMIM ID: 614921
Human Phenotype Ontology associations
Synonyms Cdg It; CDGIT; Congenital Disorders of Glycosylation, Type I; Glycogen Storage Disease Xiv; GSD14; Gsd Xiv; Pgm1 Deficiency; Phosphoglucomutase 1 Deficiency
Genes and
mouse models
There are currently no human or mouse genes associated with this disease in the MGI database.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.07
The Jackson Laboratory