arylsulfatase - CISMeF

Preferred Label : arylsulfatase;

Origin ID

F-6A550;

UMLS CUI

C0003940;

Automatic exact mappings (from CISMeF team)
- Arylsulfatase A [NCIt concept]
- Arylsulfatase a [OMIM gene]
- Cerebroside sulfatase [LOINC component]
- Cerebroside-Sulfatase [MeSH Descriptor]
- N-Acetylgalactosamine-4-Sulfatase [MeSH Descriptor]
- Steryl-Sulfatase [MeSH Descriptor]
- Sulfatase (substance) [SNOMED CT concept]
- arylsulfatase A [ORDO Gene]
- arylsulfatase A [HGNC gene]
Currated CISMeF NLP mapping
- Arylsulfatase [LOINC component]
- Arylsulfatase (substance) [SNOMED CT concept]
- arylsulfatases [MeSH concept]
- arylsulfatases [MeSH Descriptor]
Décrit
- arylsulfatase deficiency without mld [SNOMED Notion]
- arylsulfatase, total measurement [SNOMED Notion]
- metachromatic leukodystrophy, congenital type [SNOMED Notion]
- metachromatic leukodystrophy, juvenile type [SNOMED Notion]
- metachromatic leukodystrophy, late infantile type [SNOMED Notion]
- metachromatic leukodystrophy, nos [SNOMED Notion]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Enzyme [UMLS semantic type]
UMLS correspondences (same concept)
- Arylsulfatase (substance) [SNOMED CT concept]
- arylsulfatases [MeSH Descriptor]
- arylsulfatases [MeSH concept]
Validated automatic mappings to BTNT
- Cerebroside-sulfatase (substance) [SNOMED CT concept]