IGF2R, insulin like growth factor 2 receptor, 3482

N. diseases: 166; N. variants: 18
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, INSULIN-DEPENDENT, 8
disease Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome 2 0.010 None 1.000 1 2004 2004
CUI: C1335060
Disease: Non-Small Cell Adenocarcinoma
Non-Small Cell Adenocarcinoma
disease Neoplasms Neoplastic Process 5 0.200 None 1.000 1 2003 2003
Subacute progressive viral hepatitis
phenotype Finding 9 0.100 None 0
Locally Advanced Squamous Cell Carcinoma
disease Neoplastic Process 10 0.010 None 1.000 1 2003 2003
CUI: C0242973
Disease: Ventricular Dysfunction
Ventricular Dysfunction
phenotype Cardiovascular Diseases Pathologic Function 11 0.300 None 1.000 1 2019 2019
CUI: C0267812
Disease: Micronodular cirrhosis
Micronodular cirrhosis
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 18 0.100 None 0
Congenital hernia of foramen of Morgagni
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 19 0.300 None 1.000 2 2010 2011
CUI: C0553980
Disease: Endomyocardial Fibrosis
Endomyocardial Fibrosis
phenotype Cardiovascular Diseases Pathologic Function 20 0.300 None 1.000 1 2019 2019
Congenital hernia of foramen of Bochdalek
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 21 0.300 None 1.000 2 2010 2011
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement
phenotype Laboratory Procedure 23 103 0.100 None 1.000 1 1 2017 2017
CUI: C1142339
Disease: Intestinal adenoma
Intestinal adenoma
disease Neoplastic Process 23 0.010 None 1.000 1 2019 2019
CUI: C0017920
Disease: Glycogen Storage Disease Type I
Glycogen Storage Disease Type I
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 24 33 0.010 None 1.000 1 2009 2009
CUI: C0015624
Disease: Fanconi Syndrome
Fanconi Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 26 4 0.010 None 1.000 1 2008 2008
CUI: C0025309
Disease: Meningoencephalitis
Meningoencephalitis
disease Infections; Nervous System Diseases Disease or Syndrome 30 3 0.010 None 1.000 1 2018 2018
CUI: C0341703
Disease: Adult Fanconi syndrome
Adult Fanconi syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 32 0.010 None 1.000 1 2008 2008
CUI: C0003838
Disease: Arterial Occlusive Diseases
Arterial Occlusive Diseases
group Cardiovascular Diseases Disease or Syndrome 35 4 0.010 None 1.000 1 2002 2002
CUI: C0023521
Disease: Globoid cell leukodystrophy
Globoid cell leukodystrophy
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 35 111 0.010 None 1.000 1 2016 2016
Obesity-Associated Insulin Resistance
disease Disease or Syndrome 36 0.010 None 1.000 1 2019 2019
CUI: C0020725
Disease: Type II Mucolipidosis
Type II Mucolipidosis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 43 1 0.010 None 1.000 1 1992 1992
CUI: C0276548
Disease: HIV encephalitis
HIV encephalitis
disease Infections; Immune System Diseases; Nervous System Diseases; Mental Disorders Disease or Syndrome 43 0.010 None 1.000 1 2010 2010
CUI: C3839507
Disease: Diminished ovarian reserve
Diminished ovarian reserve
disease Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Disease or Syndrome 43 4 0.010 None 1.000 1 2011 2011
CUI: C0206019
Disease: HIV Encephalopathy
HIV Encephalopathy
disease Infections; Immune System Diseases; Nervous System Diseases; Mental Disorders Disease or Syndrome 45 0.010 None 1.000 1 2010 2010
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT
disease Musculoskeletal Diseases; Stomatognathic Diseases Disease or Syndrome 45 9 0.010 None 1.000 1 2018 2018
CUI: C2827469
Disease: Coronary Microvascular Disease
Coronary Microvascular Disease
disease Disease or Syndrome 45 3 0.010 None 1.000 1 2018 2018
CUI: C1709246
Disease: Non-Neoplastic Disorder
Non-Neoplastic Disorder
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 50 0.010 None 1.000 1 2019 2019