FGF2, fibroblast growth factor 2, 2247

N. diseases: 635; N. variants: 7
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: C0267370
Disease: Angiodysplasia of colon
Angiodysplasia of colon 		disease Digestive System Diseases; Cardiovascular Diseases Disease or Syndrome 6 0.010 None 1.000 1 2012 2012
CUI: C0332877
Disease: Congenital premature fusion
Congenital premature fusion 		disease Congenital Abnormality 6 1 0.010 None 1.000 1 2005 2005
CUI: C0549357
Disease: Abdominal adhesions
Abdominal adhesions 		disease Digestive System Diseases Acquired Abnormality 6 0.010 None 1.000 1 2015 2015
CUI: C0877849
Disease: Askin's tumor
Askin's tumor 		disease Neoplasms; Musculoskeletal Diseases Neoplastic Process 6 0.010 None 1.000 1 2004 2004
CUI: C0085411
Disease: Angiodysplasia
Angiodysplasia 		disease Cardiovascular Diseases Disease or Syndrome 7 0.010 None 1.000 1 2012 2012
CUI: C0392400
Disease: Diffuse malignant mesothelioma
Diffuse malignant mesothelioma 		disease Neoplasms; Respiratory Tract Diseases Neoplastic Process 7 0.010 None 1.000 1 1998 1998
CUI: C0548923
Disease: Burn infection
Burn infection 		disease Disease or Syndrome 7 0.010 None 1.000 1 2017 2017
CUI: C0687140
Disease: Hemangioma of skin
Hemangioma of skin 		disease Neoplasms; Skin and Connective Tissue Diseases; Cardiovascular Diseases Neoplastic Process 8 0.020 None 1.000 2 1995 2017
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 8 36 0.010 None 1.000 1 2001 2001
CUI: C0238577
Disease: Abdominal wall defect
Abdominal wall defect 		group Congenital Abnormality 8 0.010 None 1.000 1 2018 2018
CUI: C1335965
Disease: Signet-ring cell adenocarcinoma gastric
Signet-ring cell adenocarcinoma gastric 		disease Neoplasms Neoplastic Process 8 0.010 None 1.000 1 2018 2018
CUI: C0155668
Disease: Old myocardial infarction
Old myocardial infarction 		phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 9 0.010 None 1.000 1 2004 2004
CUI: C3489628
Disease: Thrombocytosis, Autosomal Dominant
Thrombocytosis, Autosomal Dominant 		disease Hemic and Lymphatic Diseases Disease or Syndrome 9 0.300 None 1.000 1 2005 2005
CUI: C4317006
Disease: Arthritis Pain
Arthritis Pain 		phenotype Sign or Symptom 9 0.010 None 1.000 1 2017 2017
CUI: C0684830
Disease: Secondary malignant neoplasm of axilla
Secondary malignant neoplasm of axilla 		disease Neoplastic Process 10 0.010 None 1.000 1 2003 2003
CUI: C0751117
Disease: Cryptogenic Tonic-Clonic Epilepsy
Cryptogenic Tonic-Clonic Epilepsy 		disease Nervous System Diseases Disease or Syndrome 10 0.300 None 1.000 1 2005 2005
CUI: C0751118
Disease: Epilepsy, Tonic-Clonic, Familial
Epilepsy, Tonic-Clonic, Familial 		disease Nervous System Diseases Disease or Syndrome 10 0.300 None 1.000 1 2005 2005
CUI: C0751119
Disease: Epilepsy, Tonic-Clonic, Symptomatic
Epilepsy, Tonic-Clonic, Symptomatic 		disease Nervous System Diseases Disease or Syndrome 10 0.300 None 1.000 1 2005 2005
CUI: C0036280
Disease: Burn scar
Burn scar 		disease Pathological Conditions, Signs and Symptoms; Wounds and Injuries Acquired Abnormality 11 0.010 None 1.000 1 2000 2000
CUI: C0041582
Disease: Ulcer
Ulcer 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 11 0.200 None 1.000 1 2011 2011
CUI: C0271240
Disease: Blindness of one eye (disorder)
Blindness of one eye (disorder) 		disease Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Disease or Syndrome 11 0.010 None 1.000 1 2019 2019
CUI: C1300257
Disease: Thanatophoric dysplasia, type 2
Thanatophoric dysplasia, type 2 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 11 17 0.010 None 1.000 1 2014 2014
CUI: C0039743
Disease: Thanatophoric Dysplasia
Thanatophoric Dysplasia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 12 10 0.010 None 1.000 1 1997 1997
CUI: C2721670
Disease: Ultrafiltration failure
Ultrafiltration failure 		disease Digestive System Diseases Disease or Syndrome 12 0.010 None 1.000 1 2011 2011
CUI: C0033054
Disease: Prenatal Exposure Delayed Effects
Prenatal Exposure Delayed Effects 		disease Female Urogenital Diseases and Pregnancy Complications Injury or Poisoning 13 0.300 None 1.000 1 2009 2009