MMP2, matrix metallopeptidase 2, 4313

N. diseases: 826; N. variants: 38
Source: BEFREE ×
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: C0162810
Disease: Cicatrix, Hypertrophic
Cicatrix, Hypertrophic 		disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 184 3 0.030 None 1.000 3 2010 2015
CUI: C0740391
Disease: Middle Cerebral Artery Occlusion
Middle Cerebral Artery Occlusion 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Acquired Abnormality 607 0.030 None 1.000 3 2018 2019
CUI: C0022548
Disease: Keloid
Keloid 		disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Acquired Abnormality 129 14 0.020 None 1.000 2 2008 2019
CUI: C0086543
Disease: Cataract
Cataract 		disease Eye Diseases Acquired Abnormality 385 111 0.020 None 1.000 2 1 2015 2019
CUI: C0152459
Disease: Linear atrophy
Linear atrophy 		disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 130 0.020 None 1.000 2 2017 2020
CUI: C0333293
Disease: Healing ulcer
Healing ulcer 		disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 43 1 0.020 None 1.000 2 2017 2019
CUI: C0028259
Disease: Nodule
Nodule 		phenotype Acquired Abnormality 278 19 0.010 None 1.000 1 2015 2015
CUI: C0332840
Disease: Amputated structure (morphologic abnormality)
Amputated structure (morphologic abnormality) 		phenotype Wounds and Injuries Acquired Abnormality 94 0.010 None 1.000 1 2019 2019
CUI: C0332853
Disease: Anastomosis
Anastomosis 		disease Acquired Abnormality 155 2 0.010 None 1.000 1 2017 2017
CUI: C0333307
Disease: Superficial ulcer
Superficial ulcer 		disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 242 10 0.010 None 1.000 1 2007 2007
CUI: C0341539
Disease: Parastomal hernia
Parastomal hernia 		phenotype Pathological Conditions, Signs and Symptoms Acquired Abnormality 5 0.010 None 1.000 1 2019 2019
CUI: C0410619
Disease: Prolapsed cervical intervertebral disc
Prolapsed cervical intervertebral disc 		phenotype Acquired Abnormality 2 0.010 None 1.000 1 2016 2016
CUI: C1262048
Disease: Glial scar
Glial scar 		phenotype Acquired Abnormality 51 0.010 None 1.000 1 2009 2009
CUI: C0019294
Disease: Hernia, Inguinal
Hernia, Inguinal 		phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 21 2 0.020 None 0.500 2 2018 2019
CUI: C0003855
Disease: Arteriovenous fistula
Arteriovenous fistula 		phenotype Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Anatomical Abnormality 83 8 0.210 None 1.000 1 2007 2017
CUI: C0016169
Disease: pathologic fistula
pathologic fistula 		phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 69 8 0.010 None 1.000 1 2017 2017
CUI: C0019270
Disease: Hernia
Hernia 		phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 107 9 0.010 None 1.000 1 2006 2006
CUI: C0345049
Disease: Ascending aorta dilatation
Ascending aorta dilatation 		disease Anatomical Abnormality 7 0.010 None 1.000 1 2018 2018
CUI: C0597984
Disease: Biliary stricture
Biliary stricture 		disease Digestive System Diseases Anatomical Abnormality 17 0.010 None 1.000 1 2011 2011
CUI: C0752156
Disease: Dural Arteriovenous Fistula
Dural Arteriovenous Fistula 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases Anatomical Abnormality 17 2 0.010 None 1.000 1 1 2018 2018
CUI: C3544347
Disease: Intestinal fibrosis
Intestinal fibrosis 		phenotype Anatomical Abnormality 65 0.010 None 1.000 1 2019 2019
CUI: C3889085
Disease: Ascending aortic dilatation
Ascending aortic dilatation 		phenotype Anatomical Abnormality 7 0.010 None 1.000 1 2013 2013
CUI: C0149630
Disease: Bicuspid aortic valve
Bicuspid aortic valve 		disease Cardiovascular Diseases Congenital Abnormality 103 14 0.150 None 1.000 5 2017 2019
CUI: C0003857
Disease: Congenital arteriovenous malformation
Congenital arteriovenous malformation 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 127 23 0.020 None 1.000 2 2014 2019
CUI: C0005411
Disease: Biliary Atresia
Biliary Atresia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Congenital Abnormality 169 19 0.020 None 1.000 2 2005 2005