GLIS3, GLIS family zinc finger 3, 169792

N. diseases: 105; N. variants: 48
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Endocrine System Diseases Disease or Syndrome 2 4 0.900 None 1.000 4 4 2003 2009
CUI: C0850671
Disease: Non-diabetic hyperglycemia
Non-diabetic hyperglycemia
disease Nutritional and Metabolic Diseases Disease or Syndrome 2 0.010 None 1.000 1 2017 2017
CUI: C1266049
Disease: Hyalinizing trabecular adenoma
Hyalinizing trabecular adenoma
disease Neoplasms Neoplastic Process 2 0.010 None 1.000 1 2019 2019
Thyroid Hyalinizing Trabecular Adenoma
disease Neoplasms; Endocrine System Diseases Neoplastic Process 6 0.020 None 1.000 2 2019 2019
CUI: C4020705
Disease: Glomerulocystic kidney disease
Glomerulocystic kidney disease
disease Disease or Syndrome 11 2 0.010 None 1.000 1 2009 2009
CUI: C1834931
Disease: Cystic renal dysplasia
Cystic renal dysplasia
disease Anatomical Abnormality 12 4 0.010 None 1.000 1 2017 2017
CUI: C0202231
Disease: Thyroxine measurement
Thyroxine measurement
phenotype Laboratory Procedure 24 42 0.100 None 1.000 1 1 2018 2018
CUI: C1563716
Disease: Thyroid Dysgenesis
Thyroid Dysgenesis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases Congenital Abnormality 24 5 0.010 None 1.000 1 2020 2020
CUI: C3888631
Disease: Monogenic diabetes
Monogenic diabetes
disease Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 30 19 0.010 None 1.000 1 2016 2016
CUI: C0311245
Disease: Congenital cystic kidney disease
Congenital cystic kidney disease
disease Pathological Conditions, Signs and Symptoms; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome; Congenital Abnormality 31 0.010 None 1.000 1 2009 2009
CUI: C1720164
Disease: Central corneal thickness
Central corneal thickness
phenotype Clinical Attribute 35 61 0.100 None 1.000 1 1 2018 2018
CUI: C0158981
Disease: Neonatal diabetes mellitus
Neonatal diabetes mellitus
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 42 33 0.400 None 1.000 12 2006 2018
Thyroid stimulating hormone measurement
phenotype Laboratory Procedure 42 83 0.100 None 1.000 1 1 2013 2013
CUI: C0342302
Disease: Brittle diabetes
Brittle diabetes
disease Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome 44 0.300 None 1.000 1 2009 2009
CUI: C4554117
Disease: Diabetes Mellitus, Sudden-Onset
Diabetes Mellitus, Sudden-Onset
disease Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome 44 0.300 None 1.000 1 2009 2009
Fibrolamellar Hepatocellular Carcinoma
disease Digestive System Diseases; Neoplasms Neoplastic Process 46 0.010 None 1.000 1 2019 2019
CUI: C1691228
Disease: Cystic Kidney Diseases
Cystic Kidney Diseases
group Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 50 0.030 None 1.000 3 2009 2010
CUI: C0441683
Disease: Hormone measurement
Hormone measurement
group Laboratory Procedure 51 134 0.100 None 1.000 1 1 2013 2013
CUI: C1567435
Disease: Polycystic Kidney - body part
Polycystic Kidney - body part
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Anatomical Abnormality 54 1 0.300 strong 1.000 1 2006 2006
CUI: C3837958
Disease: Diabetes Mellitus, Ketosis-Prone
Diabetes Mellitus, Ketosis-Prone
disease Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome 57 4 0.300 None 1.000 1 2009 2009
CUI: C0020302
Disease: Hydrophthalmos
Hydrophthalmos
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Congenital Abnormality 60 11 0.300 strong 1.000 1 2006 2006
CUI: C1261430
Disease: Fasting blood sugar result
Fasting blood sugar result
phenotype Laboratory or Test Result 65 113 0.100 None 1.000 2 4 2012 2012
CUI: C1518922
Disease: peak expiratory flow (procedure)
peak expiratory flow (procedure)
phenotype Laboratory Procedure 74 119 0.100 None 1.000 1 1 2019 2019
CUI: C0162671
Disease: MELAS Syndrome
MELAS Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 80 53 0.010 None 1.000 1 2012 2012
CUI: C1737329
Disease: Dysmorphism
Dysmorphism
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 80 16 0.010 None 1.000 1 2017 2017