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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Biologically Inactive Thyrotropin 
Brain-Lung-Thyroid Syndrome  
Congenital Nongoitrous Hypothyroidism +   
familial thyroid dyshormonogenesis +   
A congenital hypothyroidism characterized by thyroid hormone deficiency that is present from birth and results from defects in thyroid hormone synthesis. (DO)
Hypohidrotic Ectodermal Dysplasia, with Hypothyroidism and Agenesis of the Corpus Callosum 
Kocher-Debre-Semelaigne Syndrome 
neonatal diabetes mellitus with congenital hypothyroidism  
Ohdo syndrome, SBBYS variant  
Weaver syndrome  

Synonyms
Exact Synonyms: Thyroid Dyshormonogenesis ;   dyshormogenetic goiter ;   thyroid hormonogenesis defect
Xrefs: ORDO:95716
Definition Sources: https://pubmed.ncbi.nlm.nih.gov/15863666/ "DO" "DO"

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