leukodystrophy, metachromatic, juvenile

Preferred Label : leukodystrophy, metachromatic, juvenile;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0335514;

UMLS CUI

C0751276;

Automatic exact mappings (from CISMeF team)
- Metachromatic leukodystrophy [OMIM Phenotype]
Currated CISMeF NLP mapping
- Juvenile metachromatic leukodystrophy [ICD-11 More detail]
- Metachromatic leukodystrophy, juvenile form [ORDO Disease]
- Metachromatic leukodystrophy, juvenile type (disorder) [SNOMED CT concept]
- metachromatic leukodystrophy, juvenile type [SNOMED Notion]
Related record
- leukodystrophy, metachromatic [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Metachromatic leukodystrophy, juvenile form [ORDO Disease]
- Metachromatic leukodystrophy, juvenile type (disorder) [SNOMED CT concept]
- metachromatic leukodystrophy, juvenile type [SNOMED Notion]