spastic paraplegia 23

Preferred Label : spastic paraplegia 23;

MeSH synonym : spastic paraplegia, vitiligo, premature graying and characteristic facies; lison syndrome; spastic paraplegia and pigmentary abnormalities; abdallat davis farrage syndrome; abdallat syndrome; spastic paraparesis, vitiligo, premature graying, characteristic facies; spastic paraplegia with pigmentary abnormalities;

Details

Origin ID

C536859;

UMLS CUI

C0796019;

CISMeF manual mappings
- Autosomal recessive spastic paraplegia type 23 [ORDO Disease]
Currated CISMeF NLP mapping
- Autosomal recessive spastic paraplegia type 23 [ICD-11 More detail]
- Autosomal recessive spastic paraplegia type 23 (disorder) [SNOMED CT concept]
- Spastic paraplegia 23, autosomal recessive [OMIM Phenotype]
- hereditary spastic paraplegia 23 [DO Concept]
MeSH term(s) associated for indexing
- facies [MeSH Descriptor]
- pigmentation disorders [MeSH Descriptor]
- spastic paraplegia, hereditary [MeSH Descriptor]
- vitiligo [MeSH Descriptor]
Record concept(s)
- Spastic paraplegia 23 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal recessive spastic paraplegia type 23 [ORDO Disease]
- Autosomal recessive spastic paraplegia type 23 [ICD-11 More detail]
- Autosomal recessive spastic paraplegia type 23 (disorder) [SNOMED CT concept]
- Spastic paraplegia 23, autosomal recessive [OMIM Phenotype]
- hereditary spastic paraplegia 23 [DO Concept]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients