MMP2, matrix metallopeptidase 2, 4313

N. diseases: 1021; N. variants: 43
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: C0024950
Disease: Maxillary Diseases
Maxillary Diseases 		group Musculoskeletal Diseases; Stomatognathic Diseases Disease or Syndrome 1 0.300 None 1.000 1 2009 2009
CUI: C0029437
Disease: Idiopathic Multicentric Osteolyses
Idiopathic Multicentric Osteolyses 		disease Musculoskeletal Diseases Disease or Syndrome 1 0.010 None 1.000 1 2007 2007
CUI: C0520474
Disease: Aseptic Necrosis of Bone
Aseptic Necrosis of Bone 		phenotype Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Pathologic Function 1 0.300 None 1.000 1 2009 2009
CUI: C0741900
Disease: carcinoma sarcoma
carcinoma sarcoma 		disease Neoplastic Process 1 0.010 None 1.000 1 2011 2011
CUI: C1168331
Disease: Apical myocardial infarction
Apical myocardial infarction 		disease Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C0155100
Disease: Peripheral opacity of cornea
Peripheral opacity of cornea 		phenotype Eye Diseases Finding 1 0.100 None 0
CUI: C1850158
Disease: Interphalangeal joint erosions
Interphalangeal joint erosions 		phenotype Finding 1 0.100 None 0
CUI: C1850159
Disease: Widened metacarpal shaft
Widened metacarpal shaft 		phenotype Finding 1 0.100 None 0
CUI: C1850162
Disease: Thin metatarsal cortices
Thin metatarsal cortices 		phenotype Finding 1 0.100 None 0
CUI: C4021784
Disease: Interphalangeal joint contracture of finger
Interphalangeal joint contracture of finger 		disease Anatomical Abnormality 1 0.100 None 0
CUI: C4024729
Disease: Distal tapering of metatarsals
Distal tapering of metatarsals 		disease Anatomical Abnormality 1 0.100 None 0
CUI: C4024732
Disease: Ankylosis of feet small joints
Ankylosis of feet small joints 		disease Musculoskeletal Diseases Disease or Syndrome 1 0.100 None 0
CUI: C1850155
Disease: TORG-WINCHESTER SYNDROME
TORG-WINCHESTER SYNDROME 		disease Musculoskeletal Diseases Disease or Syndrome 2 5 0.790 strong 1.000 12 4 2001 2019
CUI: C0432289
Disease: Winchester syndrome (disorder)
Winchester syndrome (disorder) 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Musculoskeletal Diseases Disease or Syndrome 2 2 0.030 None 1.000 3 1 2005 2007
CUI: C0022682
Disease: Kienbock Disease
Kienbock Disease 		disease Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Disease or Syndrome 2 0.300 None 1.000 1 2009 2009
CUI: C0024689
Disease: Mandibular Diseases
Mandibular Diseases 		group Musculoskeletal Diseases; Stomatognathic Diseases Disease or Syndrome 2 0.300 None 1.000 1 2009 2009
CUI: C0028848
Disease: Ocular Larva Migrans
Ocular Larva Migrans 		disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C0264765
Disease: Rheumatic disease of mitral valve
Rheumatic disease of mitral valve 		disease Disease or Syndrome 2 2 0.010 None 1.000 1 1 2017 2017
CUI: C0267398
Disease: Acute ischemic colitis
Acute ischemic colitis 		phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Cardiovascular Diseases Disease or Syndrome 2 0.010 None 1.000 1 2006 2006
CUI: C0340708
Disease: Deep vein thrombosis of lower limb
Deep vein thrombosis of lower limb 		disease Cardiovascular Diseases Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C0406723
Disease: Growth retardation, Alopecia, Pseudoanodontia and Optic atrophy
Growth retardation, Alopecia, Pseudoanodontia and Optic atrophy 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Nervous System Diseases; Stomatognathic Diseases Disease or Syndrome 2 6 0.010 None 1.000 1 2015 2015
CUI: C0410619
Disease: Prolapsed cervical intervertebral disc
Prolapsed cervical intervertebral disc 		phenotype Acquired Abnormality 2 0.010 None 1.000 1 2016 2016
CUI: C0749467
Disease: Benign thyroid nodule
Benign thyroid nodule 		disease Neoplastic Process 2 0.010 None 1.000 1 2018 2018
CUI: C1834819
Disease: MYXOMATOUS MITRAL VALVE PROLAPSE 1
MYXOMATOUS MITRAL VALVE PROLAPSE 1 		disease Cardiovascular Diseases Disease or Syndrome 2 3 0.010 None 1.000 1 1 2018 2018
CUI: C1850160
Disease: Thin metacarpal cortices
Thin metacarpal cortices 		phenotype Finding 2 0.100 None 0