Dyshormogenetic goiter

Preferred Label : Dyshormogenetic goiter;

Inclusion CIM-10 : Pendred's syndrome; Familial dyshormogenetic goiter;

ICD-10 exclusion note : transitory congenital goiter with normal function (P72.0);

Diag associé à un acte (%) : 96.1;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

E071;

UMLS CUI

C0152077;

Automatic exact mappings (from CISMeF team)
- Pendred Syndrome [DO Concept]
- Pendred Syndrome [NCIt concept]
- Pendred syndrome [MeSH concept]
- Pendred syndrome [ORDO Disease]
- Pendred syndrome [MedDRA Preferred Term]
- Pendred syndrome [OMIM Phenotype]
- Pendred syndrome [PASCAL descriptor]
- Pendred's syndrome (disorder) [SNOMED CT concept]
- pendred syndrome [MeSH Supplementary Concept]
CISMeF manual mappings
- Dyshormonogenic goiter (disorder) [SNOMED CT concept]
DO Cross reference
- Pendred Syndrome [DO Concept]
- dyshormonogenic goiter [DO Concept]
Excluded by
- Other transitory neonatal endocrine disorders [ICD-10 category]
ICD-10 exclusion(s)
- Neonatal goiter, not elsewhere classified [ICD-10 Sub-category]
Orphanet concepts
- Pendred syndrome [ORDO Disease]
See also inter- (CISMeF)
- Pendred syndrome [ICD-11 Sub-sub category]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Dyshormonogenic goiter [MedDRA LLT]
- Dyshormonogenic goiter [ICD-9 code]
- Dyshormonogenic goiter (disorder) [SNOMED CT concept]
- Dyshormonogenic goitre [MedDRA LLT]
- dyshormonogenic goiter [DO Concept]

Keyword's position in hierarchy(ies) :

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