MeSH Browser

MeSH Supplementary: Thyroid Dyshormonogenesis 3
Unique ID: C562769
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562769
Entry Term(s): Hypothyroidism, Congenital, due to Dyshormonogenesis, 3; Thyroid Hormonogenesis, Genetic Defect in, 3
Registry Numbers: 0
Heading Mapped to: *Hypothyroidism; Thyroid Gland / abnormalities
Frequency: 2
Note: PROM mutation in thyroglobulin
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Thyroid Dyshormonogenesis 3 MeSH Supplementary Concept Data 2025