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: C1854610
Disease: Metacarpal osteolysis
Metacarpal osteolysis 		phenotype Finding 2 0.100 None 0
CUI: C1854614
Disease: Metatarsal osteolysis
Metatarsal osteolysis 		phenotype Finding 2 0.100 None 0
CUI: C4025195
Disease: Sclerotic cranial sutures
Sclerotic cranial sutures 		phenotype Finding 2 0.100 None 0
CUI: C0028433
Disease: Nose Neoplasms
Nose Neoplasms 		group Neoplasms; Musculoskeletal Diseases; Respiratory Tract Diseases; Otorhinolaryngologic Diseases Neoplastic Process 3 0.300 None 1.000 1 2005 2005
CUI: C0042134
Disease: Uterine hemorrhage
Uterine hemorrhage 		phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications Pathologic Function 3 0.010 None 1.000 1 2006 2006
CUI: C0751394
Disease: Cancer of Nose
Cancer of Nose 		disease Neoplasms; Musculoskeletal Diseases; Respiratory Tract Diseases; Otorhinolaryngologic Diseases Neoplastic Process 3 0.300 None 1.000 1 2005 2005
CUI: C1332353
Disease: Atypical Small Acinar Proliferation of the Prostate Gland
Atypical Small Acinar Proliferation of the Prostate Gland 		disease Neoplasms; Male Urogenital Diseases Neoplastic Process 3 0.010 None 1.000 1 2019 2019
CUI: C1659098
Disease: Complete paraplegia
Complete paraplegia 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 3 0.010 None 1.000 1 2008 2008
CUI: C1740794
Disease: Aortic wall hypertrophy
Aortic wall hypertrophy 		disease Disease or Syndrome 3 0.010 None 1.000 1 2018 2018
CUI: C1857100
Disease: Dyssegmental dysplasia
Dyssegmental dysplasia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases Disease or Syndrome 3 0.010 None 1.000 1 2003 2003
CUI: C1833734
Disease: Carpal osteolysis
Carpal osteolysis 		phenotype Pathologic Function 3 0.100 None 0
CUI: C1833735
Disease: Osteolysis involving tarsal bones
Osteolysis involving tarsal bones 		phenotype Pathologic Function 3 0.100 None 0
CUI: C1848446
Disease: C1-C2 subluxation
C1-C2 subluxation 		phenotype Finding 3 0.100 None 0
CUI: C0730271
Disease: Myopic macular degeneration
Myopic macular degeneration 		disease Eye Diseases Disease or Syndrome 4 4 0.010 None < 0.001 1 2019 2019
CUI: C0853104
Disease: Renal tubular atrophy
Renal tubular atrophy 		disease Disease or Syndrome 4 0.010 None 1.000 1 2001 2001
CUI: C1719777
Disease: Hard drusen
Hard drusen 		disease Disease or Syndrome 4 0.010 None 1.000 1 2017 2017
CUI: C0011407
Disease: Dental Pulp Necrosis
Dental Pulp Necrosis 		disease Pathological Conditions, Signs and Symptoms; Stomatognathic Diseases Disease or Syndrome 5 0.010 None 1.000 1 2017 2017
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: C0423062
Disease: Intermittent divergent squint
Intermittent divergent squint 		disease Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Disease or Syndrome 5 0.010 None 1.000 1 2020 2020
CUI: C1519675
Disease: Tumor Cell Mobility
Tumor Cell Mobility 		phenotype Neoplastic Process 5 0.010 None 1.000 1 2015 2015
CUI: C0149744
Disease: Oral lesion
Oral lesion 		phenotype Digestive System Diseases; Stomatognathic Diseases Finding 5 5 0.100 None 0 1
CUI: C0239598
Disease: Swelling of finger
Swelling of finger 		phenotype Finding 5 0.100 None 0
CUI: C4025109
Disease: Abnormal hand morphology
Abnormal hand morphology 		disease Musculoskeletal Diseases Anatomical Abnormality 5 0.100 None 0
CUI: C4025863
Disease: Abnormality of the orbital region
Abnormality of the orbital region 		phenotype Anatomical Abnormality 5 0.100 None 0
CUI: C0016033
Disease: Nonproliferative fibrocystic disease
Nonproliferative fibrocystic disease 		disease Disease or Syndrome 6 0.010 None 1.000 1 1999 1999