spastic paraplegia 38, autosomal dominant

Preferred Label : spastic paraplegia 38, autosomal dominant;

MeSH note : also known as SPG38;

Origin ID

C567349;

UMLS CUI

C2676732;

Currated CISMeF NLP mapping
- Autosomal dominant spastic paraplegia type 38 [ICD-11 More detail]
- Autosomal dominant spastic paraplegia type 38 [ORDO Disease]
- Autosomal dominant spastic paraplegia type 38 (disorder) [SNOMED CT concept]
- Spastic paraplegia 38, autosomal dominant [OMIM Phenotype]
- hereditary spastic paraplegia 38 [DO Concept]
MeSH term(s) associated for indexing
- spastic paraplegia, hereditary [MeSH Descriptor]
Record concept(s)
- spastic paraplegia 38, autosomal dominant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant spastic paraplegia type 38 [ORDO Disease]
- Autosomal dominant spastic paraplegia type 38 (disorder) [SNOMED CT concept]
- Spastic paraplegia 38, autosomal dominant [OMIM Phenotype]