hyperthyroidism, nonautoimmune

Preferred Label : hyperthyroidism, nonautoimmune;

MeSH note : mutation in TSH receptor;

MeSH synonym : toxic thyroid hyperplasia, autosomal dominant; hyperthyroidism, congenital nonautoimmune; hyperthyroidism, nonautoimmune, autosomal dominant;

Détails

Origin ID

C563786;

UMLS CUI

C1836706;

CISMeF manual mappings
- non autoimmune hyperthyroidism [Disease (Nov.)]
Currated CISMeF NLP mapping
- Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor (disorder) [SNOMED CT concept]
- Familial hyperthyroidism due to mutations in TSH receptor [ORDO Disease]
- Hereditary hyperthyroidism due to mutations in TSH receptor [ICD-11 More detail]
- Hyperthyroidism, nonautoimmune [OMIM Phenotype]
MeSH term(s) associated for indexing
- hyperthyroidism [MeSH Descriptor]
Record concept(s)
- hyperthyroidism, nonautoimmune [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial hyperthyroidism due to mutations in TSH receptor [ORDO Disease]
- Hyperthyroidism, nonautoimmune [OMIM Phenotype]

Position du mot-clé dans l'(les) arborescence(s) :

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