MeSH Browser

MeSH Supplementary: Hypothyroidism, Congenital, Nongoitrous, 5
Unique ID: C567123
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567123
Registry Number: 0
Heading Mapped to: *Congenital Hypothyroidism; Thyroid Hormones / *deficiency
Frequency: 0
Note: also known as CHNG5
Date of Entry: 2012/08/24
Revision Date: 2013/11/06

Hypothyroidism, Congenital, Nongoitrous, 5 MeSH Supplementary Concept Data 2024