metachromatic leukodystrophy, late infantile type - CISMeF

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CISMeF

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Metachromatic leukodystrophy, late infantile typeSNOMED Notion

Preferred Label : metachromatic leukodystrophy, late infantile type;

Details

Origin ID

D6-74420;

UMLS CUI

C0751278;

Currated CISMeF NLP mapping
- Late infantile metachromatic leukodystrophy [ICD-11 More detail]
- Metachromatic leukodystrophy, late infantile form [ORDO Disease]
- Metachromatic leukodystrophy, late infantile type (disorder) [SNOMED CT concept]
- infant metachromatic leukodystrophy [Disease (Nov.)]
- metachromatic leukodystrophy, infant [MeSH concept]
ICD-10 exact mapping(s)
- Other sphingolipidosis [ICD-10 Sub-category (who)]
Metaterm(s)
- metabolism [CISMeF Metaterm]
Référence SNOMED
- arylsulfatase [SNOMED Notion]
- congenital deficiency, nos [SNOMED Notion]
SNOMED CT concept
- Metachromatic leukodystrophy, late infantile type (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Late infantile metachromatic leukodystrophy [ICD-11 More detail]
- Metachromatic leukodystrophy, congenital type (disorder) [SNOMED CT concept]
- Metachromatic leukodystrophy, late infantile form [ORDO Disease]
- Metachromatic leukodystrophy, late infantile type (disorder) [SNOMED CT concept]
- infant metachromatic leukodystrophy [Disease (Nov.)]
- metachromatic leukodystrophy, infant [MeSH concept]

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02/02/2026

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