FN1, fibronectin 1, 2335

N. diseases: 724; N. variants: 33
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: C0036413
Disease: Scleredema Adultorum
Scleredema Adultorum 		disease Skin and Connective Tissue Diseases Disease or Syndrome 1 0.010 None 1.000 1 1995 1995
CUI: C0038557
Disease: Submandibular Gland Diseases
Submandibular Gland Diseases 		group Stomatognathic Diseases Disease or Syndrome 1 0.200 None 1.000 1 2009 2009
CUI: C0343263
Disease: Chondrolysis of articular cartilage
Chondrolysis of articular cartilage 		disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C0523633
Disease: Fibronectin measurement
Fibronectin measurement 		phenotype Laboratory Procedure 1 1 0.100 None 1.000 1 1 2017 2017
CUI: C0853856
Disease: Staphylococcal abscess
Staphylococcal abscess 		disease Infections Disease or Syndrome 1 0.010 None 1.000 1 2002 2002
CUI: C1866075
Disease: GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder)
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder) 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases Disease or Syndrome 1 5 0.700 strong 1.000 1 5 2008 2008
CUI: C3179037
Disease: Developmental Coxa Vara
Developmental Coxa Vara 		disease Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C4025275
Disease: Generalized distal tubular acidosis
Generalized distal tubular acidosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 1 0.100 None 0
CUI: C4025307
Disease: Hyperconvex vertebral body endplates
Hyperconvex vertebral body endplates 		phenotype Anatomical Abnormality 1 0.100 None 0
CUI: C4025733
Disease: Mesangial abnormality
Mesangial abnormality 		disease Anatomical Abnormality 1 0.100 None 0
CUI: C0432221
Disease: Spondylometaphyseal dysplasia, 'corner fracture' type
Spondylometaphyseal dysplasia, 'corner fracture' type 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Wounds and Injuries Disease or Syndrome 2 5 0.700 None 1.000 2 5 2017 2019
CUI: C0268749
Disease: Fibrillary glomerulonephritis
Fibrillary glomerulonephritis 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 2 1 0.010 None 1.000 1 1995 1995
CUI: C0852519
Disease: Benign chondrogenic neoplasm
Benign chondrogenic neoplasm 		disease Neoplasms Neoplastic Process 2 0.010 None 1.000 1 2020 2020
CUI: C1863599
Disease: Hereditary Myopathy with Early Respiratory Failure
Hereditary Myopathy with Early Respiratory Failure 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Respiratory Tract Diseases; Nervous System Diseases Disease or Syndrome 3 16 0.040 None 1.000 4 2014 2015
CUI: C0263560
Disease: Chronic ulcer of lower extremity
Chronic ulcer of lower extremity 		disease Skin and Connective Tissue Diseases Disease or Syndrome 3 0.010 None 1.000 1 2000 2000
CUI: C1288350
Disease: Subretinal membrane
Subretinal membrane 		disease Anatomical Abnormality 3 0.010 None 1.000 1 1992 1992
CUI: C1610605
Disease: Graft versus host disease in skin
Graft versus host disease in skin 		disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 3 0.010 None 1.000 1 2004 2004
CUI: C0032308
Disease: Staphylococcal Pneumonia
Staphylococcal Pneumonia 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 4 0.200 None 1.000 1 2002 2002
CUI: C0155111
Disease: Bullous keratopathy
Bullous keratopathy 		disease Eye Diseases Disease or Syndrome 4 0.010 None 1.000 1 1998 1998
CUI: C0268336
Disease: Ehlers-Danlos syndrome type 2
Ehlers-Danlos syndrome type 2 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Disease or Syndrome 4 0.010 None 1.000 1 1990 1990
CUI: C1112275
Disease: Diabetic gastroenteropathy
Diabetic gastroenteropathy 		disease Disease or Syndrome 4 0.010 None 1.000 1 2020 2020
CUI: C1142550
Disease: Native valve endocarditis
Native valve endocarditis 		disease Cardiovascular Diseases Disease or Syndrome 4 0.010 None 1.000 1 2003 2003
CUI: C3888104
Disease: Glomerulopathy with fibronectin deposits
Glomerulopathy with fibronectin deposits 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases Disease or Syndrome 5 0.570 None 1.000 8 1998 2019
CUI: C0158300
Disease: Adhesive Capsulitis
Adhesive Capsulitis 		disease Musculoskeletal Diseases Disease or Syndrome 5 0.010 None 1.000 1 2016 2016
CUI: C0268344
Disease: Ehlers-Danlos syndrome 6B
Ehlers-Danlos syndrome 6B 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 5 4 0.010 None 1.000 1 2015 2015