spastic paraplegia 3, autosomal dominant

Preferred Label : spastic paraplegia 3, autosomal dominant;

MeSH synonym : familial spastic paraplegia, autosomal dominant, 1; strumpell disease; Spastic Paraplegia 3; Spastic Paraplegia 3a; Spg3a; Spastic Paraplegia Type 3a; SPG3A Spastic paraplegia 3a; Fsp1 Familial spastic paraplegia 1;

Details

Origin ID

C536864;

UMLS CUI

C2931355;

Automatic exact mappings (from CISMeF team)
- Atlastin gtpase 1 [OMIM gene]
- Autosomal dominant spastic paraplegia type 6 (disorder) [SNOMED CT concept]
- Hereditary spastic paraplegia [MedDRA Preferred Term]
- Hereditary spastic paraplegia (disorder) [SNOMED CT concept]
- Spastic Paraplegia 3A [NCIt concept]
- Strumpell's disease [MedDRA LLT]
- hereditary spastic paraplegia 3A [DO Concept]
CISMeF manual mappings
- Autosomal dominant spastic paraplegia type 3 [ORDO Disease]
Currated CISMeF NLP mapping
- Autosomal dominant spastic paraplegia type 3 [ICD-11 More detail]
- Autosomal dominant spastic paraplegia type 3 (disorder) [SNOMED CT concept]
- Spastic paraplegia 3, autosomal dominant [OMIM Phenotype]
MeSH term(s) associated for indexing
- spastic paraplegia, hereditary [MeSH Descriptor]
ORDO relation(s)
- Autosomal dominant spastic paraplegia type 3 [ORDO Disease]
Record concept(s)
- Spastic paraplegia 3, autosomal dominant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant spastic paraplegia type 3 [ORDO Disease]
- Autosomal dominant spastic paraplegia type 3 [ICD-11 More detail]
- Autosomal dominant spastic paraplegia type 3 (disorder) [SNOMED CT concept]
- Spastic Paraplegia 3A [NCIt concept]
- Spastic paraplegia 3, autosomal dominant [OMIM Phenotype]
- Strumpell's disease [MedDRA LLT]

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