MeSH Browser

MeSH Supplementary: Thyroid Dyshormonogenesis 6
Unique ID: C564608
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564608
Entry Term(s): Hypothyroidism, Congenital, due to Dyshormonogenesis, 6; Thyroid Hormonogenesis, Genetic Defect in, 6
Registry Numbers: 0
Heading Mapped to: *Congenital Hypothyroidism
Frequency: 1
Note: mutation in DUOX2
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Thyroid Dyshormonogenesis 6 MeSH Supplementary Concept Data 2025