Disease: Hypothyroidism ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.110 GeneticVariation disease GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.110 GeneticVariation disease GWASCAT Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation. 30367059 2018
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.110 GeneticVariation disease GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.110 GeneticVariation disease GWASDB Novel associations for hypothyroidism include known autoimmune risk loci. 22493691 2012
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.110 Biomarker disease BEFREE VAV3 is involved in immune function, and FOXE1 and PTPN22 have previously been associated with hypothyroidism. 22493691 2012
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.110 GeneticVariation disease GWASCAT Novel associations for hypothyroidism include known autoimmune risk loci. 22493691 2012