TRH, thyrotropin releasing hormone, 7200

N. diseases: 230; N. variants: 2
Disease: Congenital central hypothyroidism ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4302200
Disease: Congenital central hypothyroidism
Congenital central hypothyroidism 		0.010 GeneticVariation disease BEFREE Congenital central hypothyroidism (C-CH) is a rare disease known to be caused by mutations of the genes encoding TSH β or the TRH receptor gene, although the cause of the disease in a number of patients has not yet been clarified. 23363888 2013