pendred's syndrome

Preferred Label : pendred's syndrome;

Origin ID

DB-81250;

UMLS CUI

C0271829;

Automatic exact mappings (from CISMeF team)
- Dyshormogenetic goitre [ICD-10 Sub-category (who)]
- Pendred syndrome [MedDRA Preferred Term]
Currated CISMeF NLP mapping
- Pendred Syndrome [DO Concept]
- Pendred Syndrome [NCIt concept]
- Pendred syndrome [PASCAL descriptor]
- Pendred syndrome [Disease (Nov.)]
- Pendred syndrome [ICD-11 Sub-sub category]
- Pendred syndrome [MeSH concept]
- Pendred syndrome [OMIM Phenotype]
- Pendred syndrome [ORDO Disease]
- Pendred's syndrome (disorder) [SNOMED CT concept]
- pendred syndrome [MeSH Supplementary Concept]
ICD-10 exact mapping(s)
- Dyshormogenetic goitre [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Syndromic genetic deafness [ORDO Disease]
- Syndromic hypothyroidism [ORDO Disease]
Metaterm(s)
- endocrinology [CISMeF Metaterm]
SNOMED CT concept
- Pendred's syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Pendred Syndrome [DO Concept]
- Pendred Syndrome [NCIt concept]
- Pendred syndrome [ORDO Disease]
- Pendred syndrome [MeSH concept]
- Pendred syndrome [OMIM Phenotype]
- Pendred syndrome [Disease (Nov.)]
- Pendred syndrome [PASCAL descriptor]
- Pendred syndrome [ICD-11 Sub-sub category]
- Pendred syndrome [MedDRA Preferred Term]
- Pendred's syndrome (disorder) [SNOMED CT concept]
- pendred syndrome [MeSH Supplementary Concept]