IGF2, insulin like growth factor 2, 3481

N. diseases: 604; N. variants: 19
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.
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		disease Neoplastic Process 3669 502 0.100 None 0.970 33 1996 2020
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		phenotype Neoplastic Process 6626 169 0.100 None 0.955 22 1996 2019
CUI: C0342326
Disease: Tumor-induced hypoglycemia
Tumor-induced hypoglycemia 		disease Disease or Syndrome 4 0.030 None 1.000 3 1989 1999
CUI: C1608408
Disease: Malignant transformation
Malignant transformation 		phenotype Neoplastic Process 1027 20 0.030 None 1.000 3 2009 2019
CUI: C4551836
Disease: Perilobar nephroblastomatosis
Perilobar nephroblastomatosis 		disease Neoplastic Process 3 0.030 None 1.000 3 2004 2008
CUI: C1320468
Disease: Nephrogenic rest
Nephrogenic rest 		disease Anatomical Abnormality 15 0.020 None 1.000 2 1993 1999
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		disease Disease or Syndrome 1075 276 0.020 None 0.500 2 1994 2018
CUI: C0220613
Disease: Adult Soft Tissue Sarcoma
Adult Soft Tissue Sarcoma 		disease Neoplastic Process 162 3 0.010 None 1.000 1 1999 1999
CUI: C0220645
Disease: Childhood Soft Tissue Sarcoma
Childhood Soft Tissue Sarcoma 		disease Neoplastic Process 166 3 0.010 None 1.000 1 1999 1999
CUI: C0231230
Disease: Fatigability
Fatigability 		phenotype Sign or Symptom 29 4 0.010 None 1.000 1 2005 2005
CUI: C0282666
Disease: Very Low Birth Weight
Very Low Birth Weight 		phenotype Sign or Symptom 42 2 0.010 None 1.000 1 2012 2012
CUI: C0374997
Disease: Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site 		disease Disease or Syndrome 593 24 0.010 None 1.000 1 2008 2008
CUI: C0410158
Disease: Muscle damage
Muscle damage 		phenotype Acquired Abnormality 163 4 0.010 None 1.000 1 2007 2007
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		disease Congenital Abnormality 439 617 0.010 None 1.000 1 2015 2015
CUI: C0473935
Disease: Radiolabeled somatostatin analog study
Radiolabeled somatostatin analog study 		phenotype Diagnostic Procedure 3 0.300 strong 1.000 1 2015 2015
CUI: C0678807
Disease: prenatal alcohol exposure
prenatal alcohol exposure 		phenotype Finding 5 0.300 None 1.000 1 2011 2011
CUI: C0850639
Disease: premalignant lesion
premalignant lesion 		phenotype Neoplastic Process 20 5 0.010 None 1.000 1 2009 2009
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency 		disease Disease or Syndrome 55 28 0.010 None 1.000 1 2009 2009
CUI: C0878787
Disease: Growth failure
Growth failure 		phenotype Disease or Syndrome 84 7 0.010 None < 0.001 1 2014 2014
CUI: C0940937
Disease: precancerous lesions
precancerous lesions 		phenotype Neoplastic Process 270 19 0.010 None 1.000 1 1998 1998
CUI: C1262091
Disease: Lymphocytic infiltration
Lymphocytic infiltration 		disease Disease or Syndrome 84 2 0.010 None 1.000 1 2015 2015
CUI: C1377843
Disease: Periosteal Osteosarcoma
Periosteal Osteosarcoma 		disease Neoplastic Process 5 0.010 None 1.000 1 2012 2012
CUI: C1395512
Disease: Placental dysfunction
Placental dysfunction 		disease Disease or Syndrome 31 0.010 None 1.000 1 2008 2008
CUI: C1402315
Disease: Vascular lesions
Vascular lesions 		disease Disease or Syndrome 111 9 0.010 None 1.000 1 2006 2006
CUI: C1561826
Disease: Overweight and obesity
Overweight and obesity 		disease Disease or Syndrome 81 29 0.010 None 1.000 1 2012 2012