leukodystrophy, demyelinating, Adult-Onset, autosomal dominant

Preferred Label : leukodystrophy, demyelinating, Adult-Onset, autosomal dominant;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0567113;

UMLS CUI

C1868512;

Currated CISMeF NLP mapping
- Adult onset autosomal dominant leukodystrophy (disorder) [SNOMED CT concept]
- Adult-onset autosomal dominant leukodystrophy [ICD-11 More detail]
- Adult-onset autosomal dominant leukodystrophy [ORDO Disease]
- Leukodystrophy, demyelinating, adult-onset, autosomal dominant [OMIM Phenotype]
- adult-onset autosomal dominant demyelinating leukodystrophy [DO Concept]
Related record
- leukodystrophy, demyelinating, Adult-Onset, autosomal dominant [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Adult-onset autosomal dominant leukodystrophy [ORDO Disease]
- Leukodystrophy, demyelinating, adult-onset, autosomal dominant [OMIM Phenotype]