Familial thyroid dyshormonogenesis

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Name:
Familial thyroid dyshormonogenesis
Description:
Familial thyroid dyshormonogenesis is a type of primary congenital hypothyroidism (see this term), a permanent thyroid hormone deficiency that is present from birth, which results from inborn errors of thyroid hormone synthesis.
ORPHAcode:
95716
Synonyms:
Thyroid dyshormonogenesis
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14