heparan sulfate sulfatase

Preferred Label : heparan sulfate sulfatase;

MeSH note : probable defect in Sanfilippo A syndrome;

MeSH synonym : HEPARAN SULPHATASE; heparan N-sulfatase;

Registry Number MeSH : EC 3.1.6.-;

Is substance : O;

Details

Origin ID

C021346;

UMLS CUI

C0062504;

Automatic exact mappings (from CISMeF team)
- Fanconi Anemia Group J Protein [NCIt concept]
- Fanconi Anemia Group M Protein [NCIt concept]
- General Transcription and DNA Repair Factor IIH Helicase Subunit XPD [NCIt concept]
- N-sulfoglucosamine sulfohydrolase [OMIM gene]
- RNA Helicase [NCIt concept]
- TFIIH Basal Transcription Factor Complex Helicase XPB Subunit [NCIt concept]
Currated CISMeF NLP mapping
- Heparan N-sulfatase (substance) [SNOMED CT concept]
- Heparan-N-sulfatase [LOINC component]
MeSH term(s) associated for indexing
- sulfatases [MeSH Descriptor]
Record concept(s)
- heparan sulfate sulfatase [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Enzyme [UMLS semantic type]
UMLS correspondences (same concept)
- Heparan N-sulfatase (substance) [SNOMED CT concept]
- Heparan-N-sulfatase [LOINC component]

Keyword's position in hierarchy(ies) :

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