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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
External Links
- Disease Ontology
- DOID:0111395
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- ORDO
- OMIM
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 411 | ARSB | arylsulfatase B | |
| 1103 | CHAT | choline O-acetyltransferase | |
| 2131 | EXT1 | exostosin glycosyltransferase 1 | |
| 2132 | EXT2 | exostosin glycosyltransferase 2 | |
| 2135 | EXTL2 | exostosin like glycosyltransferase 2 | |
| 2137 | EXTL3 | exostosin like glycosyltransferase 3 | |
| 2799 | GNS | glucosamine (N-acetyl)-6-sulfatase | |
| 3423 | IDS | iduronate 2-sulfatase | |
| 3425 | IDUA | alpha-L-iduronidase | |
| 4669 | NAGLU | N-acetyl-alpha-glucosaminidase |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| O43909 | Exostosin-like 3 | |
| O60502 | Protein O-GlcNAcase | |
| P15586 | N-acetylglucosamine-6-sulfatase | |
| P15848 | Arylsulfatase B | |
| P22304 | Iduronate 2-sulfatase | |
| P28329 | Choline O-acetyltransferase | |
| P35475 | Alpha-L-iduronidase | |
| P51688 | N-sulphoglucosamine sulphohydrolase | |
| P54802 | Alpha-N-acetylglucosaminidase | |
| Q16394 | Exostosin-1 |
- The Human Phenotype Ontology
| 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 |
