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: C0025211
Disease: Conjunctival melanosis
Conjunctival melanosis
disease Eye Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 1 0.010 None 1.000 1 1998 1998
CUI: C0340639
Disease: Carotid artery aneurysm
Carotid artery aneurysm
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1 0.010 None 1.000 1 2019 2019
CUI: C0524686
Disease: Periodontitis, Acute Nonsuppurative
Periodontitis, Acute Nonsuppurative
disease Stomatognathic Diseases Disease or Syndrome 1 0.300 None 1.000 1 2006 2006
CUI: C0542142
Disease: Recurrent Laryngeal Nerve Paralysis
Recurrent Laryngeal Nerve Paralysis
disease Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C1333987
Disease: Hereditary Glomangioma
Hereditary Glomangioma
disease Neoplasms Neoplastic Process 1 0.010 None 1.000 1 2002 2002
CUI: C1334687
Disease: Megakaryocytic Neoplasm
Megakaryocytic Neoplasm
disease Neoplastic Process 1 0.010 None 1.000 1 1988 1988
CUI: C4087190
Disease: Sulcus vocalis
Sulcus vocalis
disease Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C1562893
Disease: Retrocorneal fibrous membrane
Retrocorneal fibrous membrane
disease Eye Diseases Disease or Syndrome 2 0.020 None 1.000 2 2018 2019
CUI: C0040262
Disease: Tinea Versicolor
Tinea Versicolor
disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 2 0.010 None 1.000 1 2013 2013
CUI: C0410334
Disease: Defect of articular cartilage
Defect of articular cartilage
disease Anatomical Abnormality 2 0.010 None 1.000 1 2018 2018
CUI: C0008298
Disease: Polyp in nasopharynx
Polyp in nasopharynx
disease Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases Neoplastic Process 3 0.010 None 1.000 1 2006 2006
CUI: C0334473
Disease: Intramuscular lipoma
Intramuscular lipoma
disease Neoplasms Neoplastic Process 3 0.010 None 1.000 1 2017 2017
CUI: C0701824
Disease: Staggering gait
Staggering gait
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Wounds and Injuries Sign or Symptom 3 0.010 None 1.000 1 2019 2019
CUI: C3281247
Disease: BENT BONE DYSPLASIA SYNDROME
BENT BONE DYSPLASIA SYNDROME
disease Disease or Syndrome 3 10 0.010 None 1.000 1 2014 2014
CUI: C0206504
Disease: Tympanic Membrane Perforation
Tympanic Membrane Perforation
disease Otorhinolaryngologic Diseases; Wounds and Injuries Injury or Poisoning 4 0.200 None 1.000 2 1998 2010
Salivary Gland Carcinoma ex Pleomorphic Adenoma
disease Neoplastic Process 4 0.010 None 1.000 1 2010 2010
CUI: C4324434
Disease: Panniculus
Panniculus
disease Disease or Syndrome 4 0.010 None 1.000 1 2020 2020
Cataract secondary to ocular disorder
disease Eye Diseases Disease or Syndrome 5 1 0.010 None 1.000 1 2017 2017
Anterior Cerebral Circulation Infarction
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 5 0.300 None 1.000 1 2007 2007
Anterior Circulation Brain Infarction
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 5 0.300 None 1.000 1 2007 2007
Brain Infarction, Posterior Circulation
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 5 0.300 None 1.000 1 2007 2007
CUI: C0751954
Disease: Venous Infarction, Brain
Venous Infarction, Brain
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 5 0.300 None 1.000 1 2007 2007
CUI: C4087491
Disease: End stage COPD
End stage COPD
disease Disease or Syndrome 5 0.010 None 1.000 1 2017 2017
CUI: C4721766
Disease: Unspecified secondary cataract
Unspecified secondary cataract
disease Eye Diseases Disease or Syndrome 5 1 0.010 None 1.000 1 2017 2017
CUI: C0263634
Disease: Abnormal granulation tissue
Abnormal granulation tissue
phenotype Skin and Connective Tissue Diseases Sign or Symptom 6 0.010 None 1.000 1 2017 2017