Gene: TSHB ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7252
Gene Symbol: TSHB
TSHB 		0.030 GeneticVariation disease BEFREE Thyrotropin (TSH) deficiency caused by TSHβ gene mutations is a rare form of congenital central hypothyroidism. 25950606 2015
Entrez Id: 7252
Gene Symbol: TSHB
TSHB 		0.030 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
Entrez Id: 7252
Gene Symbol: TSHB
TSHB 		0.030 GeneticVariation disease BEFREE Congenital central hypothyroidism (CCH) is a rare disease which can be caused by mutations in the gene for the thyrotropin (TSH) beta subunit ( TSHB). 16804796 2006