cretinism, nos - CISMeF

CISMeF

chu

Cretinism, nosSNOMED Notion

Preferred Label : cretinism, nos;

Détails

Origin ID

D4-01830;

UMLS CUI

C0010308;

Automatic exact mappings (from CISMeF team)
- Congenital Hypothyroidism [NCIt concept]
- Congenital Iodine Deficiency Hypothyroidism [NCIt concept]
- Congenital goiter [HPO term]
- Congenital goitre [MedDRA LLT]
- Congenital hypothyroidism [HPO term]
- Congenital hypothyroidism [MedDRA Preferred Term]
- Congenital hypothyroidism [ORDO Disease]
- Congenital hypothyroidism [LOINC component]
- Congenital hypothyroidism (disorder) [SNOMED CT concept]
- Congenital hypothyroidism without goitre [ICD-10 Sub-category (who)]
- Congenital iodine deficiency syndrome (disorder) [SNOMED CT concept]
- Congenital iodine-deficiency syndrome [ICD-10 category (who)]
- Congenital iodine-deficiency syndrome, unspecified [ICD-10 Sub-category (who)]
- Cretinism [PASCAL descriptor]
- Cretinism [MedDRA LLT]
- Endemic cretinism (disorder) [SNOMED CT concept]
- GOITRE CONGENITAL [WHO-ART Preferred Term]
- Goiter congenital [MedDRA LLT]
- Goitre congenital [MedDRA Preferred Term]
- HYPOTHYROIDISM CONGENITAL [WHO-ART Preferred Term]
- Hypothyroidism congenital [MedDRA LLT]
- Neonatal goiter (disorder) [SNOMED CT concept]
- Primary congenital hypothyroidism without thyroid developmental anomaly [ORDO Disease]
- congenital anomaly endocrine/metabolic [ICPC-2 Rubric]
- congenital hypothyroidism [MeSH Descriptor]
- congenital hypothyroidism [MeSH concept]
ICD-10 exact mapping(s)
- Congenital iodine-deficiency syndrome, unspecified [ICD-10 Sub-category (who)]
Manual BTNT mappings - CISMeF
- Brain-lung-thyroid syndrome [ORDO Disease]
- Congenital hypothyroidism due to developmental anomaly [ORDO Disease]
- Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies [ORDO Disease]
- Familial thyroid dyshormonogenesis [ORDO Disease]
- Hypothyroidism due to TSH receptor mutations [ORDO Disease]
- Idiopathic congenital hypothyroidism [ORDO Disease]
- Isolated thyroid-stimulating hormone deficiency [ORDO Disease]
- Peripheral resistance to thyroid hormones [ORDO Disease]
- Transient congenital hypothyroidism [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Rare endocrine growth disease [ORDO Disease]
- Rare hypothyroidism [ORDO Disease]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
- toxicology [CISMeF Metaterm]
Référence SNOMED
- congenital deficiency, nos [SNOMED Notion]
- iodine, nos [SNOMED Notion]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital Hypothyroidism [NCIt concept]
- Congenital hypothyroidism [ICD-9 code]
- Congenital hypothyroidism [HPO term]
- Congenital hypothyroidism [ORDO Disease]
- Congenital hypothyroidism [MedDRA Preferred Term]
- Congenital hypothyroidism [LOINC component]
- Congenital hypothyroidism (disorder) [SNOMED CT concept]
- Cretinism [MedDRA LLT]
- HYPOTHYROIDISM CONGENITAL [WHO-ART Preferred Term]
- Hypothyroidism congenital [MedDRA LLT]
- congenital hypothyroidism [MeSH Descriptor]
- congenital hypothyroidism [MeSH concept]
- congenital hypothyroidism [Disease (Nov.)]
- congenital hypothyroidism [DO Concept]
Validated automatic mappings to NTBT
- Congenital hypothyroidism [ICD-11 Subcategory]

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26/07/2025

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