Autosomal recessive spastic paraplegia type 18 - CISMeF

" /> Autosomal recessive spastic paraplegia type 18 - CISMeF

CISMeF

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Autosomal recessive spastic paraplegia type 18ICD-11 More detail

Preferred Label : Autosomal recessive spastic paraplegia type 18;

Details

Origin ID

429795598;

UMLS CUI

C2749936;

Currated CISMeF NLP mapping
- Autosomal recessive spastic paraplegia type 18 [ORDO Disease]
- Autosomal recessive spastic paraplegia type 18 (disorder) [SNOMED CT concept]
- Spastic paraplegia 18b, autosomal recessive [OMIM Phenotype]
- hereditary spastic paraplegia 18 [DO Concept]
- spastic paraplegia 18, autosomal recessive [MeSH concept]
- spastic paraplegia 18, autosomal recessive [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal recessive spastic paraplegia type 18 [ORDO Disease]
- Autosomal recessive spastic paraplegia type 18 (disorder) [SNOMED CT concept]
- Spastic paraplegia 18b, autosomal recessive [OMIM Phenotype]
- hereditary spastic paraplegia 18 [DO Concept]
- spastic paraplegia 18, autosomal recessive [MeSH concept]
- spastic paraplegia 18, autosomal recessive [MeSH Supplementary Concept]

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17/06/2025

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