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: C0005818
Disease: Blood Platelet Disorders
Blood Platelet Disorders
group Hemic and Lymphatic Diseases Disease or Syndrome 59 5 0.010 None 1.000 1 1996 1996
CUI: C0023652
Disease: Lichen Sclerosus et Atrophicus
Lichen Sclerosus et Atrophicus
disease Skin and Connective Tissue Diseases Disease or Syndrome 64 2 0.010 None 1.000 1 2012 2012
Chronic rejection of renal transplant
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 64 1 0.010 None 1.000 1 2006 2006
CUI: C3544347
Disease: Intestinal fibrosis
Intestinal fibrosis
phenotype Anatomical Abnormality 65 0.020 None 1.000 2 2017 2017
CUI: C0002390
Disease: Extrinsic allergic alveolitis
Extrinsic allergic alveolitis
group Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 65 2 0.010 None 1.000 1 2014 2014
Autoimmune Lymphoproliferative Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 65 22 0.010 None 1.000 1 2014 2014
CUI: C0155094
Disease: Corneal pannus
Corneal pannus
disease Pathological Conditions, Signs and Symptoms; Eye Diseases Disease or Syndrome 66 0.010 None 1.000 1 1999 1999
CUI: C3203547
Disease: Axial spondyloarthritis
Axial spondyloarthritis
disease Musculoskeletal Diseases Disease or Syndrome 67 0.010 None 1.000 1 2019 2019
CUI: C0007273
Disease: Carotid Artery Diseases
Carotid Artery Diseases
group Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 69 6 0.010 None 1.000 1 2013 2013
Secondary malignant neoplasm of pancreas
disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 69 4 0.010 None 1.000 1 2005 2005
CUI: C0010495
Disease: Cutis Laxa
Cutis Laxa
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 70 21 0.010 None 1.000 1 2005 2005
CUI: C0343284
Disease: Chondrodysplasia
Chondrodysplasia
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 71 1 0.020 None 1.000 2 2014 2018
CUI: C0267952
Disease: Fibrosis of pancreas
Fibrosis of pancreas
disease Digestive System Diseases Disease or Syndrome 72 0.010 None 1.000 1 2018 2018
CUI: C1840311
Disease: Laryngeal cleft
Laryngeal cleft
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 72 4 0.010 None 1.000 1 2018 2018
CUI: C0281899
Disease: Prolapsed lumbar disc
Prolapsed lumbar disc
disease Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Acquired Abnormality 75 33 0.010 None 1.000 1 2008 2008
CUI: C0035328
Disease: Retinal Vein Occlusion
Retinal Vein Occlusion
disease Eye Diseases; Cardiovascular Diseases Disease or Syndrome 76 15 0.010 None 1.000 1 2003 2003
CUI: C0013720
Disease: Ehlers-Danlos Syndrome
Ehlers-Danlos Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Disease or Syndrome 77 14 0.010 None 1.000 1 2012 2012
CUI: C0042025
Disease: Urinary Stress Incontinence
Urinary Stress Incontinence
disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 79 5 0.020 None 1.000 2 2010 2011
CUI: C0018824
Disease: Heart valve disease
Heart valve disease
group Cardiovascular Diseases Disease or Syndrome 79 5 0.010 None 1.000 1 2010 2010
Arrhythmogenic Right Ventricular Dysplasia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome; Congenital Abnormality 82 136 0.010 None 1.000 1 2017 2017
CUI: C0035869
Disease: Rotavirus Infections
Rotavirus Infections
group Infections Disease or Syndrome 84 0.010 None 1.000 1 2004 2004
CUI: C0595936
Disease: Aqueous Humor Disorders
Aqueous Humor Disorders
disease Eye Diseases Disease or Syndrome 85 1 0.020 None 1.000 2 2016 2016
CUI: C0584960
Disease: Factor V Leiden mutation
Factor V Leiden mutation
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 86 46 0.010 None 1.000 1 2006 2006
CUI: C0008149
Disease: Chlamydia Infections
Chlamydia Infections
group Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases Disease or Syndrome 88 10 0.010 None 1.000 1 2018 2018
CUI: C1279945
Disease: Acute interstitial pneumonia
Acute interstitial pneumonia
disease Respiratory Tract Diseases Disease or Syndrome 88 8 0.010 None 1.000 1 2018 2018