spastic paraplegia 13, autosomal dominant

Preferred Label : spastic paraplegia 13, autosomal dominant;

Origin ID

C537485;

UMLS CUI

C1854467;

Automatic exact mappings (from CISMeF team)
- hereditary spastic paraplegia 13 [DO Concept]
CISMeF manual mappings
- Autosomal dominant spastic paraplegia type 13 [ORDO Disease]
Currated CISMeF NLP mapping
- Autosomal dominant spastic paraplegia type 13 [ICD-11 More detail]
- Autosomal dominant spastic paraplegia type 13 (disorder) [SNOMED CT concept]
- Spastic paraplegia 13, autosomal dominant [OMIM Phenotype]
MeSH term(s) associated for indexing
- spastic paraplegia, hereditary [MeSH Descriptor]
ORDO relation(s)
- Autosomal dominant spastic paraplegia type 13 [ORDO Disease]
Record concept(s)
- Spastic paraplegia 13, autosomal dominant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant spastic paraplegia type 13 [ORDO Disease]
- Autosomal dominant spastic paraplegia type 13 [ICD-11 More detail]
- Autosomal dominant spastic paraplegia type 13 (disorder) [SNOMED CT concept]
- Spastic paraplegia 13, autosomal dominant [OMIM Phenotype]