MeSH Browser

MeSH Supplementary: Thyroid Dyshormonogenesis 4
Unique ID: C562770
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562770
Entry Term(s): Deiodinase Deficiency; Hypothyroidism, Congenital, due to Dyshormonogenesis, 4; Iodotyrosine Dehalogenase Deficiency; Thyroid Hormonogenesis, Genetic Defect in, 4
Registry Numbers: 0
Heading Mapped to: *Congenital Hypothyroidism; Hydrolases / deficiency; Iodide Peroxidase / deficiency
Frequency: 3
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Thyroid Dyshormonogenesis 4 MeSH Supplementary Concept Data 2025