mucopolysaccharidosis type IIID

Summary
Synonym
  • GNS deficiency
  • MPS IIID
  • MPS3D
  • Mucopolysaccharidosis type 3D
  • N-acetylglucosamine-6-sulfatase deficiency
  • Sanfilippo syndrome D
  • Sanfilippo syndrome type D
Definition
A mucopolysaccharidosis III that has_material_basis_in homozygous or compound heterozygous mutation in GNS on chromosome 12q14.3.
Super Class
autosomal recessive disease mucopolysaccharidosis III
Disease Ontology
DOID:0111402
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
GARD
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
2799 GNS glucosamine (N-acetyl)-6-sulfatase
6448 SGSH N-sulfoglucosamine sulfohydrolase
Displaying 1 entry
Gene ID Gene Symbol Description Source
75612 Gns glucosamine (N-acetyl)-6-sulfatase
Related Glycoprotein
The Human Phenotype Ontology
Displaying entries 21 - 30 of 69 in total
HPO ID HPO Term
HP:0000713 Agitation
HP:0000718 Aggressive behavior
HP:0000750 Delayed speech and language development
HP:0000752 Hyperactivity
HP:0000900 Thickened ribs
HP:0000943 Dysostosis multiplex
HP:0001007 Hirsutism
HP:0001169 Broad palm
HP:0001249 Intellectual disability
HP:0001250 Seizure
Displaying 1 entry
Gene ID Gene Symbol Description
2799 GNS glucosamine (N-acetyl)-6-sulfatase

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024