spastic paraplegia 2, X-linked

Preferred Label : spastic paraplegia 2, X-linked;

Origin ID

C536857;

UMLS CUI

C1839264;

CISMeF manual mappings
- Spastic paraplegia type 2 [ORDO Disease]
Currated CISMeF NLP mapping
- Spastic paraplegia 2, X-linked [OMIM Phenotype]
- X-linked spastic paraplegia type 2 [ICD-11 More detail]
- X-linked spastic paraplegia type 2 (disorder) [SNOMED CT concept]
- hereditary spastic paraplegia 2 [DO Concept]
MeSH term(s) associated for indexing
- genetic diseases, X-linked [MeSH Descriptor]
- spastic paraplegia, hereditary [MeSH Descriptor]
ORDO relation(s)
- Spastic paraplegia type 2 [ORDO Disease]
Record concept(s)
- Spastic paraplegia 2, X-linked [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Spastic paraplegia 2, X-linked [OMIM Phenotype]
- Spastic paraplegia type 2 [ORDO Disease]
- X-linked spastic paraplegia type 2 (disorder) [SNOMED CT concept]