Pseudo-Hurler polydystrophy Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Mucolipidosis III alpha/beta (MLIII alpha/beta) is a lysosomal disorder characterized by progressive slowing of the growth rate from early childhood, stiffness and pain in joints, gradual coarsening of facial features, moderate developmental delay and mild intellectual disability in most patients. (Orphanet Rare Disease Ontology, Orphanet_577)
External Link http://www.omim.org/entry/252600
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Genes

1 genes associated with the Pseudo-Hurler polydystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits