spastic paraplegia 36, autosomal dominant

Preferred Label : spastic paraplegia 36, autosomal dominant;

MeSH note : also known as SPG36;

MeSH synonym : Spg36;

Origin ID

C567930;

UMLS CUI

C2936879;

Currated CISMeF NLP mapping
- Autosomal dominant spastic paraplegia type 36 [ORDO Disease]
- Autosomal dominant spastic paraplegia type 36 (disorder) [SNOMED CT concept]
- Spastic paraplegia 36, autosomal dominant [OMIM Phenotype]
- hereditary spastic paraplegia 36 [DO Concept]
MeSH term(s) associated for indexing
- spastic paraplegia, hereditary [MeSH Descriptor]
Record concept(s)
- spastic paraplegia 36, autosomal dominant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant spastic paraplegia type 36 [ORDO Disease]
- Autosomal dominant spastic paraplegia type 36 (disorder) [SNOMED CT concept]
- Spastic paraplegia 36, autosomal dominant [OMIM Phenotype]