spastic paraplegia 14, autosomal recessive - CISMeF

CISMeF

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Spastic paraplegia 14, autosomal recessiveMeSH Supplementary Concept

Preferred Label : spastic paraplegia 14, autosomal recessive;

Details

Origin ID

C537486;

UMLS CUI

C1854568;

CISMeF manual mappings
- Autosomal recessive spastic paraplegia type 14 [ORDO Disease]
Currated CISMeF NLP mapping
- Autosomal recessive spastic paraplegia type 14 [ICD-11 More detail]
- Autosomal recessive spastic paraplegia type 14 (disorder) [SNOMED CT concept]
- Spastic paraplegia 14, autosomal recessive [OMIM Phenotype]
- hereditary spastic paraplegia 14 [DO Concept]
MeSH term(s) associated for indexing
- intellectual disability [MeSH Descriptor]
- spastic paraplegia, hereditary [MeSH Descriptor]
ORDO relation(s)
- Autosomal recessive spastic paraplegia type 14 [ORDO Disease]
Record concept(s)
- Spastic paraplegia 14, autosomal recessive [MeSH concept]
See also inter- (CISMeF)
- spastic paraplegia 14 (autosomal recessive) [ORDO Gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal recessive spastic paraplegia type 14 [ORDO Disease]
- Autosomal recessive spastic paraplegia type 14 [ICD-11 More detail]
- Autosomal recessive spastic paraplegia type 14 (disorder) [SNOMED CT concept]
- Spastic paraplegia 14, autosomal recessive [OMIM Phenotype]
- hereditary spastic paraplegia 14 [DO Concept]

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16/06/2024

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