MeSH Browser

MeSH Supplementary: Thyroid Dyshormonogenesis 5
Unique ID: C562771
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562771
Entry Term(s): Hypothyroidism, Congenital, due to Dyshormonogenesis, 5; Thyroid Hormonogenesis, Genetic Defect in, 5
Registry Numbers: 0
Heading Mapped to: *Hypothyroidism; Thyroid Gland / abnormalities
Frequency: 0
Note: mutation in DUOXA2
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Thyroid Dyshormonogenesis 5 MeSH Supplementary Concept Data 2025