pseudoarylsulfatase A deficiency - CISMeF

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CISMeF

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Pseudoarylsulfatase A deficiencyMeSH Supplementary Concept

Preferred Label : pseudoarylsulfatase A deficiency;

MeSH note : mutation in arylsulfatase A;

Details

Origin ID

C565403;

UMLS CUI

C1855255;

Currated CISMeF NLP mapping
- Metachromatic leukodystrophy [OMIM Phenotype]
- Metachromatic leukodystrophy [ORDO Disease]
- Pseudoarylsulfatase A deficiency [ORDO Disease]
MeSH term(s) associated for indexing
- arylsulfatases [MeSH Descriptor]
- leukodystrophy, metachromatic [MeSH Descriptor]
Record concept(s)
- pseudoarylsulfatase A deficiency [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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25/05/2025

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