MeSH Browser

MeSH Supplementary: Hyperthyroidism, Familial Gestational
Unique ID: C566384
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566384
Registry Numbers: 0
Heading Mapped to: *Hyperthyroidism; *Pregnancy Complications; Receptors, Thyrotropin / deficiency
Frequency: 1
Note: associated with mutation in TSHR gene
Date of Entry: 2012/08/24
Revision Date: 2013/11/06

Hyperthyroidism, Familial Gestational MeSH Supplementary Concept Data 2025