hypermethioninemia, nos - CISMeF

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CISMeF

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Hypermethioninemia, nosSNOMED Notion

Preferred Label : hypermethioninemia, nos;

Details

Origin ID

D6-B4300;

UMLS CUI

C0268621;

Currated CISMeF NLP mapping
- Hypermethioninaemia [MedDRA Preferred Term]
- Hypermethioninemia [PASCAL descriptor]
- Hypermethioninemia [MeSH Supplementary Concept]
- Hypermethioninemia [HPO term]
- Hypermethioninemia [MedDRA LLT]
- Hypermethioninemia (disorder) [SNOMED CT concept]
- Methioninaemia [ICD-11 More detail]
- hypermethioninemia [MeSH concept]
- hypermethioninemia [DO Concept]
- hypermethioninemia [Disease (Nov.)]
ICD-10 exact mapping(s)
- Disorders of sulfur-bearing amino-acid metabolism [ICD-10 Sub-category (who)]
Metaterm(s)
- metabolism [CISMeF Metaterm]
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Hypermethioninemia (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Brain demyelination due to methionine adenosyltransferase deficiency [ORDO Disease]
- Brain demyelination due to methionine adenosyltransferase deficiency [ICD-11 More detail]
- Deficiency of methionine adenosyltransferase (disorder) [SNOMED CT concept]
- Hepatic methionine adenosyltransferase deficiency (disorder) [SNOMED CT concept]
- Hypermethioninemia [HPO term]
- Methionine Adenosyltransferase Deficiency [NCIt concept]
- Methionine adenosyltransferase I/iii deficiency [OMIM Phenotype]
- hypermethioninemia [MeSH concept]
- methionine adenosyltransferase deficiency [MeSH concept]

Keyword's position in hierarchy(ies) :

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22/05/2025

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