IGF1, insulin like growth factor 1, 3479

N. diseases: 1206; N. variants: 36
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: C0151482
Disease: Megaloblastic anemia due to folate deficiency
Megaloblastic anemia due to folate deficiency 		disease Hemic and Lymphatic Diseases Disease or Syndrome 1 0.200 None 1.000 1 2006 2006
CUI: C0242012
Disease: NEPHROTIC SYNDROME, CHRONIC
NEPHROTIC SYNDROME, CHRONIC 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C0339678
Disease: Simple myopia
Simple myopia 		disease Eye Diseases Disease or Syndrome 1 2 0.010 None 1.000 1 2 2016 2016
CUI: C0423693
Disease: Growing pains
Growing pains 		phenotype Sign or Symptom 1 0.010 None 1.000 1 2018 2018
CUI: C0748534
Disease: sciatic nerve inflammation
sciatic nerve inflammation 		disease Disease or Syndrome 1 0.010 None < 0.001 1 2018 2018
CUI: C1096352
Disease: Pancreatic enlargement
Pancreatic enlargement 		disease Disease or Syndrome 1 0.010 None 1.000 1 2008 2008
CUI: C4022604
Disease: Glomerulomegaly
Glomerulomegaly 		disease Disease or Syndrome 1 0.010 None 1.000 1 2019 2019
CUI: C0202220
Disease: Somatomedin-C measurement
Somatomedin-C measurement 		phenotype Laboratory Procedure 1 0.300 strong 0
CUI: C0271547
Disease: Overproduction of growth hormone
Overproduction of growth hormone 		disease Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 2 0.030 None 1.000 3 1999 2018
CUI: C0153999
Disease: Benign neoplasm of uterus
Benign neoplasm of uterus 		disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 2 0.010 None 1.000 1 2002 2002
CUI: C0281913
Disease: Swelling of skeletal muscle
Swelling of skeletal muscle 		disease Disease or Syndrome 2 0.010 None 1.000 1 2018 2018
CUI: C0342337
Disease: Insulin resistance - type B
Insulin resistance - type B 		disease Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C2713546
Disease: Androgen Receptor Deficiency
Androgen Receptor Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 2 0.010 None 1.000 1 2013 2013
CUI: C4552322
Disease: Obesity cardiomyopathy
Obesity cardiomyopathy 		disease Cardiovascular Diseases Disease or Syndrome 2 0.010 None 1.000 1 2020 2020
CUI: C4755297
Disease: Somatomammotropinoma
Somatomammotropinoma 		disease Neoplastic Process 2 0.010 None 1.000 1 2018 2018
CUI: C0752149
Disease: Headache, Intractable
Headache, Intractable 		disease Nervous System Diseases Disease or Syndrome 3 0.010 None 1.000 1 2018 2018
CUI: C0795855
Disease: Ring chromosome 15 syndrome
Ring chromosome 15 syndrome 		disease Disease or Syndrome 3 0.010 None 1.000 1 1999 1999
CUI: C1334620
Disease: Malignant Smooth Muscle Neoplasm
Malignant Smooth Muscle Neoplasm 		disease Neoplasms; Musculoskeletal Diseases Neoplastic Process 3 0.010 None 1.000 1 1990 1990
CUI: C4274352
Disease: Chronic intestinal failure
Chronic intestinal failure 		disease Disease or Syndrome 3 0.010 None 1.000 1 2019 2019
CUI: C4318479
Disease: Growth Hormone Insensitivity Syndrome
Growth Hormone Insensitivity Syndrome 		phenotype Pathological Conditions, Signs and Symptoms Disease or Syndrome 4 1 0.060 None 1.000 6 1999 2013
CUI: C0271695
Disease: Rabson-Mendenhall Syndrome
Rabson-Mendenhall Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Endocrine System Diseases Disease or Syndrome 4 11 0.020 None 1.000 2 2001 2007
CUI: C0014008
Disease: Empty Sella Syndrome
Empty Sella Syndrome 		disease Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 4 0.010 None 1.000 1 1998 1998
CUI: C0020494
Disease: Hyperostosis Frontalis Interna
Hyperostosis Frontalis Interna 		disease Musculoskeletal Diseases Disease or Syndrome 4 0.010 None 1.000 1 2017 2017
CUI: C1842839
Disease: HYPOTRICHOSIS 6
HYPOTRICHOSIS 6 		disease Skin and Connective Tissue Diseases Disease or Syndrome 4 7 0.010 None 1.000 1 2015 2015
CUI: C1836264
Disease: Congenital bilateral ptosis
Congenital bilateral ptosis 		disease Congenital Abnormality 4 1 0.100 None 0