hyperthyroidism, familial gestational

Preferred Label : hyperthyroidism, familial gestational;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0566684;

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]
Related record
- hyperthyroidism, familial gestational [MeSH Supplementary 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]