hyperthyroidism, familial gestational

Preferred Label : hyperthyroidism, familial gestational;

MeSH note : associated with mutation in TSHR gene;

Origin ID

C566384;

UMLS CUI

C1863959;

Currated CISMeF NLP mapping
- Familial gestational hyperthyroidism [ICD-11 More detail]
- Familial gestational hyperthyroidism [ORDO Disease]
- Familial gestational hyperthyroidism (disorder) [SNOMED CT concept]
- Hyperthyroidism, familial gestational [OMIM Phenotype]
MeSH term(s) associated for indexing
- hyperthyroidism [MeSH Descriptor]
- pregnancy complications [MeSH Descriptor]
- receptors, thyrotropin [MeSH Descriptor]
ORDO relation(s)
- Familial gestational hyperthyroidism [ORDO Disease]
Record concept(s)
- hyperthyroidism, familial gestational [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial gestational hyperthyroidism [ORDO Disease]
- Familial gestational hyperthyroidism [ICD-11 More detail]
- Familial gestational hyperthyroidism (disorder) [SNOMED CT concept]
- Hyperthyroidism, familial gestational [OMIM Phenotype]