GLIS3, GLIS family zinc finger 3, 169792

N. diseases: 105; N. variants: 48
Disease: Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1857775
Disease: Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism
Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism 		0.900 Biomarker disease GENOMICS_ENGLAND
CUI: C1857775
Disease: Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism
Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism 		0.900 CausalMutation disease CLINVAR
CUI: C1857775
Disease: Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism
Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism 		0.900 Biomarker disease CTD_human
CUI: C1857775
Disease: Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism
Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism 		0.900 Biomarker disease GENOMICS_ENGLAND
CUI: C1857775
Disease: Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism
Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism 		0.900 Biomarker disease MGD A murine model of neonatal diabetes mellitus in Glis3-deficient mice. 19481545 2009
CUI: C1857775
Disease: Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism
Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism 		0.900 Biomarker disease MGD Glis3 is associated with primary cilia and Wwtr1/TAZ and implicated in polycystic kidney disease. 19273592 2009
CUI: C1857775
Disease: Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism
Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism 		0.900 Biomarker disease GENOMICS_ENGLAND Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism. 16715098 2006
CUI: C1857775
Disease: Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism
Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism 		0.900 GermlineCausalMutation disease ORPHANET Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism. 16715098 2006
CUI: C1857775
Disease: Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism
Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism 		0.900 Biomarker disease GENOMICS_ENGLAND Neonatal diabetes mellitus, congenital hypothyroidism, hepatic fibrosis, polycystic kidneys, and congenital glaucoma: a new autosomal recessive syndrome? 12966531 2003