peutz-jeghers syndrome

Preferred Label : peutz-jeghers syndrome;

Détails

Origin ID

D4-01035;

UMLS CUI

C0031269;

Currated CISMeF NLP mapping
- Peutz Jeghers syndrome [Disease (Nov.)]
- Peutz-Jeghers Syndrome [NCIt concept]
- Peutz-Jeghers syndrome [PASCAL descriptor]
- Peutz-Jeghers syndrome [DO Concept]
- Peutz-Jeghers syndrome [ICD-11 Subcategory]
- Peutz-Jeghers syndrome [MeSH concept]
- Peutz-Jeghers syndrome [MedDRA Preferred Term]
- Peutz-Jeghers syndrome [ORDO Disease]
- Peutz-Jeghers syndrome (disorder) [SNOMED CT concept]
- Peutz-jeghers syndrome [OMIM Phenotype]
- peutz-jeghers syndrome [MeSH Descriptor]
ICD-10 exact mapping(s)
- Other phakomatoses, not elsewhere classified [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Genetic hyperpigmentation of the skin [ORDO Disease]
- Hyperpigmentation of the skin [ORDO Disease]
- Malformation syndrome with hamartosis [ORDO Disease]
- Palpebral lentiginosis [ORDO Disease]
- Pigmented conjunctival lesion [ORDO Disease]
- Polymalformative genetic syndrome with increased risk of developing cancer [ORDO Disease]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Peutz-Jeghers syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Peutz Jeghers syndrome [Disease (Nov.)]
- Peutz-Jeghers Syndrome [NCIt concept]
- Peutz-Jeghers syndrome [ORDO Disease]
- Peutz-Jeghers syndrome [MedDRA Preferred Term]
- Peutz-Jeghers syndrome [MeSH concept]
- Peutz-Jeghers syndrome [DO Concept]
- Peutz-Jeghers syndrome [PASCAL descriptor]
- Peutz-Jeghers syndrome (disorder) [SNOMED CT concept]
- Peutz-jeghers syndrome [OMIM Phenotype]
- peutz-jeghers syndrome [MeSH Descriptor]

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