N-sulfoglucosamine sulfohydrolase

Preferred Label : N-sulfoglucosamine sulfohydrolase;

Approved symbol HGNC : SGSH;

Name synonyms HGNC : mucopolysaccharidosis type IIIA; sulfamidase;

Alias symbols HGNC : HSS; MPS3A; SFMD;

Chromosome HGNC : 17q25.3;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000181523;

Details

Origin ID

HGNC:10818;

UMLS CUI

C1420015;

Automatic exact mappings (from CISMeF team)
- Hallermann-streiff syndrome [OMIM Phenotype]
- Mucopolysaccharidosis III-A (disorder) [SNOMED CT concept]
- Mucopolysaccharidosis, type iiia [OMIM Phenotype]
- N-Sulfoglucosamine sulfohydrolase (substance) [SNOMED CT concept]
- N-sulfoglucosamine sulfohydrolase [ORDO Gene]
- N-sulfoglucosamine sulfohydrolase [OMIM gene]
- N-sulfoglucosamine sulfohydrolase [MeSH concept]
- N-sulfoglucosamine sulfohydrolase [MeSH Supplementary Concept]
- Sanfilippo syndrome type A [ORDO Disease]
- mucopolysaccharidosis iii [MeSH Descriptor]
- mucopolysaccharidosis type IIIA [DO Concept]
- n-sulfoglucosamine sulfohydrolase [SNOMED Notion]
NCIt concept
- SGSH Gene [NCIt concept]
OMIM gene
- N-sulfoglucosamine sulfohydrolase [OMIM gene]
Orphanet gene
- N-sulfoglucosamine sulfohydrolase [ORDO Gene]
See also inter- (CISMeF)
- Mucopolysaccharidosis Type IIIA [NCIt concept]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- N-sulfoglucosamine sulfohydrolase [OMIM gene]
- SGSH gene [LOINC component]

Keyword's position in hierarchy(ies) :

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