spastic paraplegia 6, autosomal dominant

Preferred Label : spastic paraplegia 6, autosomal dominant;

MeSH note : Fsp3; Spg6 not included;

MeSH synonym : familial spastic paraplegia, autosomal dominant 3; Spg6; Fsp3; familial spastic paraplegia, autosomal dominant, 3;

Details

Origin ID

C536866;

UMLS CUI

C1838192;

CISMeF manual mappings
- Autosomal dominant spastic paraplegia type 6 [ORDO Disease]
Currated CISMeF NLP mapping
- Autosomal dominant spastic paraplegia type 6 [ICD-11 More detail]
- Autosomal dominant spastic paraplegia type 6 (disorder) [SNOMED CT concept]
- Spastic paraplegia 6, autosomal dominant [OMIM Phenotype]
- hereditary spastic paraplegia 6 [DO Concept]
MeSH term(s) associated for indexing
- spastic paraplegia, hereditary [MeSH Descriptor]
ORDO relation(s)
- Autosomal dominant spastic paraplegia type 6 [ORDO Disease]
Record concept(s)
- Spastic paraplegia 6, autosomal dominant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant spastic paraplegia type 6 [ORDO Disease]
- Autosomal dominant spastic paraplegia type 6 (disorder) [SNOMED CT concept]
- Spastic paraplegia 6, autosomal dominant [OMIM Phenotype]

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