Arylsulfatase a

Preferred Label : Arylsulfatase a;

Symbol : ARSA;

CISMeF acronym : ARSA;

Type : Gene;

Alternative titles and symbols : Cerebroside 3-sulfatase; CEREBROSIDE-SULFATASE;

Ensembl ID : ENSG00000100299;

Prefixed ID : *607574;

Details

Origin ID

607574;

UMLS CUI

C1412553;

Automatic exact mappings (from CISMeF team)
- Aberrant origin of right subclavian artery [ICD-11 More detail]
- Arylsulfatase [LOINC component]
- Arylsulfatase (substance) [SNOMED CT concept]
- Arylsulfatase A [NCIt concept]
- Autosomal recessive sideroblastic anemia [ORDO Disease]
- Cerebroside sulfatase [LOINC component]
- Cerebroside-Sulfatase [MeSH concept]
- Cerebroside-Sulfatase [MeSH Descriptor]
- Cerebroside-sulfatase (substance) [SNOMED CT concept]
- arylsulfatase [SNOMED Notion]
- arylsulfatase A [ORDO Gene]
- arylsulfatase A [HGNC gene]
- arylsulfatases [MeSH Descriptor]
- arylsulfatases [MeSH concept]
- cerebroside-sulfatase [SNOMED Notion]
Currated CISMeF NLP mapping
- ARSA Gene [NCIt concept]
- ARSA gene [LOINC component]
HGNC gene
- arylsulfatase A [HGNC gene]
NCIt concept(s)
- ARSA Gene [NCIt concept]
- ARSA wt Allele [NCIt concept]
- Arylsulfatase A [NCIt concept]
ORDO concept(s)
- arylsulfatase A [ORDO Gene]
Phenotypes related
- Metachromatic leukodystrophy [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- ARSA Gene [NCIt concept]
- ARSA gene [LOINC component]
- arylsulfatase A [HGNC gene]

Keyword's position in hierarchy(ies) :

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