papillon-lefevre syndrome - CISMeF

CISMeF

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Papillon-lefevre syndromeSNOMED Notion

Preferred Label : papillon-lefevre syndrome;

Details

Origin ID

D4-40137;

UMLS CUI

C0030360;

Automatic exact mappings (from CISMeF team)
- Papillon-Lefevre syndrome [MedDRA Preferred Term]
Currated CISMeF NLP mapping
- Papillon-Lefevre Syndrome [NCIt concept]
- Papillon-Lefevre disease [MeSH concept]
- Papillon-Lefèvre syndrome [ICD-11 More detail]
- Papillon-Lefèvre syndrome [ORDO Disease]
- Papillon-Lefèvre syndrome (disorder) [SNOMED CT concept]
- Papillon-lefevre syndrome [OMIM Phenotype]
- papillon-lefevre disease [MeSH Descriptor]
ICD-10 exact mapping(s)
- Other specified congenital malformations of skin [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Autosomal recessive isolated diffuse palmoplantar keratoderma [ORDO Disease]
- Ectodermal dysplasia syndrome [ORDO Disease]
- Functional neutrophil defect [ORDO Disease]
- Genetic malformation syndrome with odontal and/or periodontal component [ORDO Disease]
- Hereditary palmoplantar keratoderma [ORDO Disease]
- Malformation syndrome with odontal and/or periodontal component [ORDO Disease]
- Zlotogura-Martinez syndrome [ORDO Disease]
Metaterm(s)
- dermatology [CISMeF Metaterm]
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Papillon-Lefèvre syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Papillon-Lefevre Syndrome [NCIt concept]
- Papillon-Lefevre disease [MeSH concept]
- Papillon-Lefevre disease [Disease (Nov.)]
- Papillon-Lefevre disease [DO Concept]
- Papillon-Lefevre syndrome [MedDRA Preferred Term]
- Papillon-Lefèvre syndrome [ORDO Disease]
- Papillon-Lefèvre syndrome [ICD-11 More detail]
- Papillon-Lefèvre syndrome (disorder) [SNOMED CT concept]
- Papillon-lefevre syndrome [OMIM Phenotype]
- papillon-lefevre disease [MeSH Descriptor]

Keyword's position in hierarchy(ies) :

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19/05/2024

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