MeSH Browser

MeSH Supplementary: Hypothyroidism, Congenital, Nongoitrous, 2
Unique ID: C566852
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566852
Entry Term(s): Athyreotic Hypothyroidism; Hypothyroidism, Athyreotic; Hypothyroidism, Congenital, Due To Thyroid Dysgenesis
Registry Numbers: 0
Heading Mapped to: *Congenital Hypothyroidism; *Thyroid Dysgenesis
Frequency: 22
Note: also known as CHNG2; associated with mutatins in PAX8
Date of Entry: 2012/08/24
Revision Date: 1955/01/01

Hypothyroidism, Congenital, Nongoitrous, 2 MeSH Supplementary Concept Data 2025