leukodystrophy, dysmyelinating, and spastic paraparesis with or without dystonia

Preferred Label : leukodystrophy, dysmyelinating, and spastic paraparesis with or without dystonia;

Origin ID

C567311;

UMLS CUI

C3496228;

Currated CISMeF NLP mapping
- Autosomal recessive spastic paraplegia type 35 [ORDO Disease]
- Autosomal recessive spastic paraplegia type 35 [ICD-11 More detail]
- Autosomal recessive spastic paraplegia type 35 (disorder) [SNOMED CT concept]
- Spastic paraplegia 35, autosomal recessive, with or without neurodegeneration [OMIM Phenotype]
- hereditary spastic paraplegia 35 [DO Concept]
MeSH term(s) associated for indexing
- spastic paraplegia, hereditary [MeSH Descriptor]
Record concept(s)
- leukodystrophy, dysmyelinating, and spastic paraparesis with or without dystonia [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal recessive spastic paraplegia type 35 [ORDO Disease]
- Autosomal recessive spastic paraplegia type 35 [ICD-11 More detail]
- Autosomal recessive spastic paraplegia type 35 (disorder) [SNOMED CT concept]
- Spastic paraplegia 35, autosomal recessive, with or without neurodegeneration [OMIM Phenotype]
- hereditary spastic paraplegia 35 [DO Concept]