MMRN1, multimerin 1, 22915

N. diseases: 272; N. variants: 3
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: C0264515
Disease: Pneumonia, Necrotizing
Pneumonia, Necrotizing 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 3 0.010 None 1.000 1 2004 2004
CUI: C4699511
Disease: Stroke of undetermined etiology
Stroke of undetermined etiology 		disease Disease or Syndrome 3 0.010 None 1.000 1 2007 2007
CUI: C0269972
Disease: Postpartum cardiomyopathy
Postpartum cardiomyopathy 		disease Cardiovascular Diseases Disease or Syndrome 5 0.010 None 1.000 1 2018 2018
CUI: C0015499
Disease: Hereditary Factor V Deficiency
Hereditary Factor V Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 7 7 0.010 None 1.000 1 1996 1996
CUI: C0410787
Disease: Hereditary Connective Tissue Disorder
Hereditary Connective Tissue Disorder 		group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 9 0.010 None 1.000 1 2005 2005
CUI: C1850959
Disease: Corneal dystrophy, Fuchs' endothelial, 1
Corneal dystrophy, Fuchs' endothelial, 1 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 9 7 0.010 None 1.000 1 2019 2019
CUI: C0741250
Disease: aspirin sensitivity
aspirin sensitivity 		phenotype Disease or Syndrome 10 0.010 None 1.000 1 2018 2018
CUI: C0812437
Disease: Oculo-dento-digital syndrome
Oculo-dento-digital syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Musculoskeletal Diseases; Stomatognathic Diseases Congenital Abnormality 12 22 0.010 None 1.000 1 2015 2015
CUI: C3854603
Disease: FNAITP
FNAITP 		disease Disease or Syndrome 12 2 0.010 None 1.000 1 2011 2011
CUI: C0334565
Disease: Adenoameloblastoma
Adenoameloblastoma 		disease Neoplasms Neoplastic Process 19 2 0.010 None 1.000 1 2010 2010
CUI: C0410538
Disease: Pseudoachondroplasia
Pseudoachondroplasia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 19 16 0.010 None 1.000 1 2009 2009
CUI: C0473527
Disease: Hypoalphalipoproteinemias
Hypoalphalipoproteinemias 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 20 7 0.010 None 1.000 1 2006 2006
CUI: C1444680
Disease: Posterior capsule opacification
Posterior capsule opacification 		disease Eye Diseases Disease or Syndrome 20 0.010 None 1.000 1 2018 2018
CUI: C0684686
Disease: Secondary malignant neoplasm of soft tissues
Secondary malignant neoplasm of soft tissues 		group Neoplasms Neoplastic Process 22 0.010 None 1.000 1 2017 2017
CUI: C0242006
Disease: Myelofibrosis due to another disorder
Myelofibrosis due to another disorder 		disease Disease or Syndrome 23 6 0.010 None 1.000 1 1998 1998
CUI: C4302896
Disease: Hormone sensitive prostate cancer
Hormone sensitive prostate cancer 		disease Neoplasms; Male Urogenital Diseases Neoplastic Process 27 0.010 None 1.000 1 2019 2019
CUI: C0948187
Disease: Tracheomalacia
Tracheomalacia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Respiratory Tract Diseases Disease or Syndrome 30 5 0.010 None 1.000 1 2019 2019
CUI: C2350344
Disease: Chronic Lung Injury
Chronic Lung Injury 		disease Respiratory Tract Diseases; Wounds and Injuries Disease or Syndrome 33 0.010 None 1.000 1 2019 2019
CUI: C1306889
Disease: Peripheral arterial occlusive disease
Peripheral arterial occlusive disease 		disease Cardiovascular Diseases Disease or Syndrome 35 3 0.010 None 1.000 1 2013 2013
CUI: C0002438
Disease: Amebiasis
Amebiasis 		disease Infections Disease or Syndrome 37 2 0.010 None 1.000 1 2019 2019
CUI: C1704356
Disease: Enchondroma
Enchondroma 		disease Neoplasms Neoplastic Process 41 13 0.010 None 1.000 1 2017 2017
CUI: C0013370
Disease: Amebic colitis
Amebic colitis 		disease Digestive System Diseases; Infections Disease or Syndrome 49 1 0.010 None 1.000 1 2019 2019
CUI: C0259785
Disease: Malignant Meningioma
Malignant Meningioma 		disease Neoplasms; Nervous System Diseases Neoplastic Process 49 0.010 None 1.000 1 2012 2012
CUI: C1262048
Disease: Glial scar
Glial scar 		phenotype Acquired Abnormality 51 0.010 None 1.000 1 2018 2018
CUI: C0019104
Disease: Hemorrhagic Fevers, Viral
Hemorrhagic Fevers, Viral 		disease Infections Disease or Syndrome 57 0.010 None 1.000 1 2013 2013