spastic paraplegia 7, autosomal recessive

Preferred Label : spastic paraplegia 7, autosomal recessive;

MeSH note : mutation in the paraplegin gene, SPG7;

Origin ID

C564599;

UMLS CUI

C1846564;

Currated CISMeF NLP mapping
- Autosomal recessive spastic paraplegia type 7 [ICD-11 More detail]
- Spastic Paraplegia 7 [NCIt concept]
- Spastic paraplegia 7, autosomal recessive [OMIM Phenotype]
- Spastic paraplegia type 7 [ORDO Disease]
- Spastic paraplegia type 7 (disorder) [SNOMED CT concept]
- hereditary spastic paraplegia 7 [DO Concept]
MeSH term(s) associated for indexing
- spastic paraplegia, hereditary [MeSH Descriptor]
Record concept(s)
- spastic paraplegia 7, autosomal recessive [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Spastic Paraplegia 7 [NCIt concept]
- Spastic paraplegia 7, autosomal recessive [OMIM Phenotype]
- Spastic paraplegia type 7 [ORDO Disease]