Congenital malformations of other endocrine glands

Preferred Label : Congenital malformations of other endocrine glands;

Inclusion CIM-10 : Congenital malformation of parathyroid or thyroid gland; Thyroglossal cyst; Persistent thyroglossal duct;

ICD-10 exclusion note : congenital goiter (E03.0); congenital hypothyroidism (E03.1);

Associé à un acte opératoire (%) : 90.0;

Diag associé à un acte (%) : 97.7;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

Q892;

UMLS CUI

C0432378;

Automatic exact mappings (from CISMeF team)
- Persistent Thyroglossal Duct [NCIt concept]
- Persistent thyroglossal duct (disorder) [SNOMED CT concept]
- Thyroglossal Duct Cyst [NCIt concept]
- Thyroglossal cyst [ICD-11 More detail]
- Thyroglossal cyst [HPO term]
- Thyroglossal cyst [MedDRA Preferred Term]
- Thyroglossal duct cyst (disorder) [SNOMED CT concept]
- thyroglossal cyst [MeSH Descriptor]
- thyroglossal cyst [MeSH concept]
Orphanet concepts
- Congenital thyroid malformation without hypothyroidism [ORDO Disease]
- Duplication of the pituitary gland [ORDO Disease]
- Familial thyroglossal duct cyst [ORDO Disease]
- Thyroglossal duct cyst [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Anomalies of other endocrine glands [ICD-9 code]

Keyword's position in hierarchy(ies) :

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