spastic paraplegia 31, autosomal dominant

Preferred Label : spastic paraplegia 31, autosomal dominant;

MeSH note : also known as SPG31; associated with mutations in REEP1 gene;

Origin ID

C565210;

UMLS CUI

C1853247;

Currated CISMeF NLP mapping
- Autosomal dominant spastic paraplegia type 31 [ICD-11 More detail]
- Autosomal dominant spastic paraplegia type 31 [ORDO Disease]
- Autosomal dominant spastic paraplegia type 31 (disorder) [SNOMED CT concept]
- Spastic Paraplegia 31 [NCIt concept]
- Spastic paraplegia 31, autosomal dominant [OMIM Phenotype]
- hereditary spastic paraplegia 31 [DO Concept]
MeSH term(s) associated for indexing
- spastic paraplegia, hereditary [MeSH Descriptor]
Record concept(s)
- spastic paraplegia 31, autosomal dominant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant spastic paraplegia type 31 [ORDO Disease]
- Autosomal dominant spastic paraplegia type 31 (disorder) [SNOMED CT concept]
- Spastic Paraplegia 31 [NCIt concept]
- Spastic paraplegia 31, autosomal dominant [OMIM Phenotype]