MMP2, matrix metallopeptidase 2, 4313

N. diseases: 628; N. variants: 23
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: C0028259
Disease: Nodule
Nodule
phenotype Acquired Abnormality 125 8 0.010 1.000 1 2016 2016
CUI: C0156181
Disease: Peritoneal adhesion
Peritoneal adhesion
phenotype Acquired Abnormality 21 0.010 1.000 1 2008 2008
CUI: C0333463
Disease: Senile Plaques
Senile Plaques
phenotype Pathological Conditions, Signs and Symptoms Acquired Abnormality 300 27 0.010 1.000 1 2010 2010
CUI: C2936349
Disease: Plaque, Amyloid
Plaque, Amyloid
phenotype Pathological Conditions, Signs and Symptoms Acquired Abnormality 234 23 0.010 1.000 1 2010 2010
CUI: C2936380
Disease: Neointima
Neointima
phenotype Pathological Conditions, Signs and Symptoms Acquired Abnormality 5 0.300 1 2008 2008
CUI: C0264133
Disease: Acquired flat foot
Acquired flat foot
phenotype Acquired Abnormality 103 0.100 0
CUI: C0409345
Disease: Flexion contracture - wrist
Flexion contracture - wrist
phenotype Acquired Abnormality 7 0.100 0
CUI: C0409354
Disease: Flexion contracture of hip
Flexion contracture of hip
phenotype Acquired Abnormality 21 0.100 0
CUI: C0002940
Disease: Aneurysm
Aneurysm
phenotype Cardiovascular Diseases Anatomical Abnormality 151 7 0.100 1.000 11 1999 2010
CUI: C0019270
Disease: Hernia
Hernia
phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 41 6 0.010 1.000 1 2006 2006
CUI: C0032584
Disease: polyps
polyps
phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 284 19 0.010 1 2008 2008
CUI: C0597984
Disease: Biliary stricture
Biliary stricture
phenotype Anatomical Abnormality 16 0.010 1.000 1 2012 2012
CUI: C0016202
Disease: Flatfoot
Flatfoot
phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Anatomical Abnormality 107 4 0.100 0
CUI: C0409495
Disease: Protrusio acetabuli
Protrusio acetabuli
phenotype Anatomical Abnormality 8 1 0.100 0
CUI: C0575158
Disease: Kyphoscoliosis deformity of spine
Kyphoscoliosis deformity of spine
phenotype Anatomical Abnormality 83 1 0.100 0
CUI: C1857130
Disease: Hypoplastic mandible condyle
Hypoplastic mandible condyle
phenotype Anatomical Abnormality 394 0.100 0
CUI: C4021774
Disease: Camptodactyly of toe
Camptodactyly of toe
phenotype Anatomical Abnormality 8 0.100 0
Interphalangeal joint contracture of finger
phenotype Anatomical Abnormality 1 0.100 0
CUI: C4021797
Disease: Abnormality of the thorax
Abnormality of the thorax
phenotype Anatomical Abnormality 22 0.100 0
CUI: C4024589
Disease: Aplasia/Hypoplasia of the mandible
Aplasia/Hypoplasia of the mandible
phenotype Anatomical Abnormality 396 0.100 0
CUI: C4024729
Disease: Distal tapering of metatarsals
Distal tapering of metatarsals
phenotype Anatomical Abnormality 1 0.100 0
CUI: C4476523
Disease: Decreased projection of lower jaw
Decreased projection of lower jaw
phenotype Anatomical Abnormality 394 0.100 0
CUI: C4476524
Disease: Decreased projection of mandible
Decreased projection of mandible
phenotype Anatomical Abnormality 394 0.100 0
CUI: C4476525
Disease: Retrusion of lower jaw
Retrusion of lower jaw
phenotype Anatomical Abnormality 394 0.100 0
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 186 4 0.300 2 2007 2007