MMP3, matrix metallopeptidase 3, 4314

N. diseases: 473; N. variants: 24
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: C1290590
Disease: Hyperplastic tooth follicle
Hyperplastic tooth follicle 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases Congenital Abnormality 1 0.010 None 1.000 1 2008 2008
CUI: C0263778
Disease: Chronic osteoarthritis
Chronic osteoarthritis 		disease Musculoskeletal Diseases Disease or Syndrome 2 0.010 None 1.000 1 2017 2017
CUI: C1504568
Disease: Stenosis of middle cerebral artery
Stenosis of middle cerebral artery 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 2 0.010 None 1.000 1 2011 2011
CUI: C1333843
Disease: Grade 3 Invasive Breast Carcinoma
Grade 3 Invasive Breast Carcinoma 		disease Neoplastic Process 3 0.010 None 1.000 1 2008 2008
CUI: C0154051
Disease: Hemangioma of retina
Hemangioma of retina 		disease Neoplasms; Eye Diseases; Cardiovascular Diseases Neoplastic Process 4 0.010 None 1.000 1 2009 2009
CUI: C1168305
Disease: Corneal melt
Corneal melt 		disease Disease or Syndrome 4 0.010 None 1.000 1 2003 2003
CUI: C1384641
Disease: Cervical spondylosis
Cervical spondylosis 		disease Musculoskeletal Diseases Disease or Syndrome 4 1 0.010 None 1.000 1 2018 2018
CUI: C1696153
Disease: Remitting seronegative symmetrical synovitis with pitting oedema syndrome
Remitting seronegative symmetrical synovitis with pitting oedema syndrome 		disease Disease or Syndrome 4 0.010 None 1.000 1 2018 2018
CUI: C1366911
Disease: Cerebral Cavernous Malformations 1
Cerebral Cavernous Malformations 1 		disease Disease or Syndrome 5 7 0.010 None 1.000 1 2016 2016
CUI: C1566302
Disease: Preterm Premature Rupture of Fetal Membranes
Preterm Premature Rupture of Fetal Membranes 		disease Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 5 0.010 None 1.000 1 1999 1999
CUI: C0339229
Disease: Superior limbic keratoconjunctivitis
Superior limbic keratoconjunctivitis 		disease Eye Diseases Disease or Syndrome 6 0.010 None 1.000 1 2011 2011
CUI: C0341299
Disease: Collagenous Sprue
Collagenous Sprue 		disease Digestive System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome 6 0.010 None 1.000 1 2006 2006
CUI: C0017567
Disease: Gingival Hypertrophy
Gingival Hypertrophy 		disease Stomatognathic Diseases Disease or Syndrome 7 0.010 None 1.000 1 2010 2010
CUI: C0741975
Disease: carotid disease
carotid disease 		disease Disease or Syndrome 7 5 0.010 None < 0.001 1 2004 2004
CUI: C0745581
Disease: knee symptoms
knee symptoms 		phenotype Sign or Symptom 7 0.010 None 1.000 1 2017 2017
CUI: C3266123
Disease: Serrated polyp
Serrated polyp 		disease Pathological Conditions, Signs and Symptoms Anatomical Abnormality 7 0.010 None 1.000 1 2019 2019
CUI: C0878693
Disease: Conjunctivochalasis
Conjunctivochalasis 		disease Eye Diseases Disease or Syndrome 9 0.030 None 1.000 3 2000 2017
CUI: C0237938
Disease: Gastrointestinal ulcer
Gastrointestinal ulcer 		disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 9 0.010 None 1.000 1 1996 1996
CUI: C0340766
Disease: Venous hypertension
Venous hypertension 		disease Disease or Syndrome 9 0.010 None 1.000 1 2018 2018
CUI: C0406632
Disease: Autoimmune skin disease
Autoimmune skin disease 		disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 9 0.010 None 1.000 1 2019 2019
CUI: C1866956
Disease: Aortic root dilation
Aortic root dilation 		disease Disease or Syndrome 9 0.010 None 1.000 1 2011 2011
CUI: C0024959
Disease: Maxillary Sinusitis
Maxillary Sinusitis 		disease Infections; Respiratory Tract Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 10 0.010 None 1.000 1 2017 2017
CUI: C0032453
Disease: Polychondritis, Relapsing
Polychondritis, Relapsing 		disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 10 0.010 None 1.000 1 2018 2018
CUI: C0746025
Disease: Lumbar spondylolisthesis
Lumbar spondylolisthesis 		phenotype Musculoskeletal Diseases Acquired Abnormality 10 0.010 None 1.000 1 2009 2009
CUI: C0012359
Disease: Pathological Dilatation
Pathological Dilatation 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 11 0.010 None 1.000 1 2008 2008