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: C0022548
Disease: Keloid
Keloid 		disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Acquired Abnormality 165 15 0.040 None 1.000 4 1992 2019
CUI: C0086543
Disease: Cataract
Cataract 		disease Eye Diseases Acquired Abnormality 878 124 0.040 None 1.000 4 1999 2018
CUI: C1519666
Disease: Tumor-Associated Vasculature
Tumor-Associated Vasculature 		disease Acquired Abnormality 84 0.040 None 1.000 4 2010 2019
CUI: C0162810
Disease: Cicatrix, Hypertrophic
Cicatrix, Hypertrophic 		disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 185 3 0.030 None 1.000 3 1996 2017
CUI: C0028259
Disease: Nodule
Nodule 		phenotype Acquired Abnormality 278 19 0.020 None 1.000 2 2017 2017
CUI: C0152459
Disease: Linear atrophy
Linear atrophy 		disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 149 6 0.020 None 1.000 2 1994 2018
CUI: C0339543
Disease: Epiretinal Membrane
Epiretinal Membrane 		disease Eye Diseases Acquired Abnormality 102 0.020 None 1.000 2 1992 2009
CUI: C0015826
Disease: Fenestration (morphologic abnormality)
Fenestration (morphologic abnormality) 		disease Acquired Abnormality 43 0.010 None 1.000 1 2008 2008
CUI: C0333161
Disease: Pseudocyst
Pseudocyst 		disease Pathological Conditions, Signs and Symptoms; Neoplasms Acquired Abnormality 8 0.010 None 1.000 1 1999 1999
CUI: C1262048
Disease: Glial scar
Glial scar 		phenotype Acquired Abnormality 51 0.010 None 1.000 1 2018 2018
CUI: C1297883
Disease: Radial scar
Radial scar 		disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 10 0.010 None 1.000 1 2002 2002
CUI: C0009917
Disease: Contracture
Contracture 		disease Musculoskeletal Diseases Anatomical Abnormality 111 12 0.020 None 1.000 2 2019 2019
CUI: C1260954
Disease: Morphologically altered structure
Morphologically altered structure 		disease Anatomical Abnormality 46 0.020 None 1.000 2 2010 2019
CUI: C1285498
Disease: Vegetation
Vegetation 		disease Anatomical Abnormality 67 0.020 None 1.000 2 2001 2013
CUI: C0019270
Disease: Hernia
Hernia 		phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 136 10 0.010 None 1.000 1 2019 2019
CUI: C0029866
Disease: Other ureteric obstruction
Other ureteric obstruction 		phenotype Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Anatomical Abnormality 52 0.200 None 1.000 1 2002 2002
CUI: C1288350
Disease: Subretinal membrane
Subretinal membrane 		disease Anatomical Abnormality 3 0.010 None 1.000 1 1992 1992
CUI: C0016202
Disease: Flatfoot
Flatfoot 		phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Anatomical Abnormality 285 38 0.100 None 0
CUI: C0022821
Disease: Kyphosis deformity of spine
Kyphosis deformity of spine 		phenotype Musculoskeletal Diseases Anatomical Abnormality 305 10 0.100 None 0
CUI: C0576093
Disease: Knee joint valgus deformity
Knee joint valgus deformity 		disease Musculoskeletal Diseases Anatomical Abnormality 117 5 0.100 None 0
CUI: C4021744
Disease: Abnormality of the wrist
Abnormality of the wrist 		disease Anatomical Abnormality 10 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: C0871470
Disease: Systolic Pressure
Systolic Pressure 		phenotype Clinical Attribute 843 1931 0.100 None 1.000 3 2 2017 2019
CUI: C0042834
Disease: Vital capacity
Vital capacity 		phenotype Clinical Attribute 430 746 0.100 None 1.000 1 1 2019 2019