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Thyroid Dyshormonogenesis 3 MeSH Supplementary Concept Data 2024


MeSH Supplementary
Thyroid Dyshormonogenesis 3
Unique ID
C562769
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C562769
Entry Term(s)
Hypothyroidism, Congenital, due to Dyshormonogenesis, 3
Thyroid Hormonogenesis, Genetic Defect in, 3
Registry Number
0
Heading Mapped to
*Hypothyroidism
Thyroid Gland / *abnormalities
Frequency
2
Note
PROM mutation in thyroglobulin
Date of Entry
2012/11/05
Revision Date
2013/11/06
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