SLC30A10, solute carrier family 30 member 10, 55532

N. diseases: 120; N. variants: 22
Disease: Central hypothyroidism ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0271801
Disease: Central hypothyroidism
Central hypothyroidism 		0.300 Biomarker disease CTD_human Hypothyroidism induced by loss of the manganese efflux transporter SLC30A10 may be explained by reduced thyroxine production. 28860195 2017