Congenital hypothyroidism with diffuse goiter

Preferred Label : Congenital hypothyroidism with diffuse goiter;

Inclusion CIM-10 : Congenital parenchymatous goiter (nontoxic); Congenital goiter (nontoxic) NOS;

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

Diag associé à un acte (%) : 74.2;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

E030;

UMLS CUI

C0342149;

Currated CISMeF NLP mapping
- Congenital hypothyroidism with diffuse goiter (disorder) [SNOMED CT concept]
- Congenital hypothyroidism with diffuse goitre [ICD-10 Sub-category (who)]
- Permanent congenital hypothyroidism with diffuse goitre [ICD-11 Sub-sub category]
Excluded by
- Other nontoxic goiter [ICD-10 category]
- Other transitory neonatal endocrine disorders [ICD-10 category]
ICD-10 exclusion(s)
- Neonatal goiter, not elsewhere classified [ICD-10 Sub-category]
Orphanet concepts
- Congenital hypothyroidism [ORDO Disease]
- Familial thyroid dyshormonogenesis [ORDO Disease]
- Peripheral resistance to thyroid hormones [ORDO Disease]
- Permanent congenital hypothyroidism [ORDO Disease]
- Primary congenital hypothyroidism [ORDO Disease]
- Primary congenital hypothyroidism without thyroid developmental anomaly [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital Hypothyroidism with Diffuse Goiter [NCIt concept]
- Congenital hypothyroidism with diffuse goiter (disorder) [SNOMED CT concept]
- Permanent congenital hypothyroidism with diffuse goitre [ICD-11 Sub-sub category]

Keyword's position in hierarchy(ies) :

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