Gene: HESX1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8820
Gene Symbol: HESX1
HESX1 		0.410 Biomarker disease GENOMICS_ENGLAND Recent advances in central congenital hypothyroidism. 26416826 2015
Entrez Id: 8820
Gene Symbol: HESX1
HESX1 		0.410 GeneticVariation disease BEFREE In conclusion, a de novo heterozygous frameshift mutation in exon 2 of the HESX1 causes severe CPHD with optic nerve hypoplasia in a human. 12519827 2003
Entrez Id: 8820
Gene Symbol: HESX1
HESX1 		0.410 Biomarker disease HPO