mucopolysaccharidosis type IIIA

Summary
Synonym
  • MPS3A
  • MPSIIIA
  • Sanfilippo syndrome type A
  • heparan sulfamidase deficiency
  • mucopolysaccharidosis III-A
  • mucopolysaccharidosis type 3A
  • mucopolysaccharidosis type IIIA (Sanfilippo A)
Definition
A mucopolysaccharidosis III characterized by severe clinical manifestation and earlier age of onset compared to other forms of mucopolysaccharidosis III that has_material_basis_in homozygous or compound heterozygous mutation in the SGSH gene on chromosome 17q25.3.
Super Class
autosomal recessive disease mucopolysaccharidosis III
Disease Ontology
DOID:0111395
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
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
27029 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase)
The Human Phenotype Ontology
Displaying entries 11 - 20 of 27 in total
HPO ID HPO Term
HP:0003309 Ovoid thoracolumbar vertebrae
HP:0001007 Hirsutism
HP:0001744 Splenomegaly
HP:0000007 Autosomal recessive inheritance
HP:0001263 Global developmental delay
HP:0002208 Coarse hair
HP:0000365 Hearing impairment
HP:0002788 Recurrent upper respiratory tract infections
HP:0000943 Dysostosis multiplex
HP:0001670 Asymmetric septal hypertrophy
Displaying 1 entry
Gene ID Gene Symbol Description
6448 SGSH N-sulfoglucosamine sulfohydrolase

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Acknowledgements

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Last updated: December 9, 2024