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: C0576093
Disease: Knee joint valgus deformity
Knee joint valgus deformity
disease Musculoskeletal Diseases Anatomical Abnormality 117 5 0.100 None 0
CUI: C1838662
Disease: Metaphyseal irregularity
Metaphyseal irregularity
phenotype Finding 34 0.100 None 0
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
disease Musculoskeletal Diseases Disease or Syndrome 850 135 0.100 None 0
CUI: C4521256
Disease: Glomerulopathy Assessment
Glomerulopathy Assessment
phenotype Diagnostic Procedure 84 0.100 None 0
CUI: C0040015
Disease: Thrombasthenia
Thrombasthenia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 48 61 0.010 None < 0.001 1 1982 1982
CUI: C0005283
Disease: beta Thalassemia
beta Thalassemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 198 103 0.010 None 1.000 1 1984 1984
CUI: C3841475
Disease: beta^+^ Thalassemia
beta^+^ Thalassemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 156 44 0.010 None 1.000 1 1984 1984
CUI: C1305968
Disease: Eccrine dermal cylindroma
Eccrine dermal cylindroma
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 12 3 0.010 None 1.000 1 1985 1985
CUI: C0472803
Disease: Hypodysfibrinogenemia
Hypodysfibrinogenemia
disease Disease or Syndrome 8 1 0.010 None 1.000 1 1985 1985
CUI: C1368683
Disease: Epithelioma
Epithelioma
disease Neoplasms Neoplastic Process 326 2 0.010 None 1.000 1 1988 1988
CUI: C1290886
Disease: Chronic inflammatory disorder
Chronic inflammatory disorder
group Pathological Conditions, Signs and Symptoms Disease or Syndrome 74 0.010 None 1.000 1 1988 1988
CUI: C3163918
Disease: Tumor thrombus
Tumor thrombus
phenotype Cardiovascular Diseases Disease or Syndrome 50 3 0.010 None 1.000 1 1989 1989
Liver and Intrahepatic Biliary Tract Carcinoma
disease Digestive System Diseases; Neoplasms Neoplastic Process 1395 73 0.020 None 1.000 2 1989 1990
CUI: C0345904
Disease: Malignant neoplasm of liver
Malignant neoplasm of liver
disease Digestive System Diseases; Neoplasms Neoplastic Process 1649 88 0.020 None 1.000 2 1989 1990
CUI: C0220630
Disease: Adult Liver Carcinoma
Adult Liver Carcinoma
disease Digestive System Diseases; Neoplasms Neoplastic Process 1377 72 0.020 None 1.000 2 1989 1990
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: C0085179
Disease: Eosinophilia-Myalgia Syndrome
Eosinophilia-Myalgia Syndrome
disease Musculoskeletal Diseases; Nervous System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 10 0.010 None 1.000 1 1991 1991
CUI: C0206659
Disease: Embryonal Carcinoma
Embryonal Carcinoma
disease Neoplasms Neoplastic Process 165 0.010 None 1.000 1 1991 1991
CUI: C0079474
Disease: Hallopeau-Siemens Disease
Hallopeau-Siemens Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 51 54 0.010 None 1.000 1 1992 1992
Respiratory Distress Syndrome, Adult
disease Respiratory Tract Diseases Disease or Syndrome 434 60 0.010 None 1.000 1 1992 1992
CUI: C1288350
Disease: Subretinal membrane
Subretinal membrane
disease Anatomical Abnormality 3 0.010 None 1.000 1 1992 1992
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 441 120 0.010 None 1.000 1 1992 1992
CUI: C0852283
Disease: Respiratory Distress Syndrome
Respiratory Distress Syndrome
disease Disease or Syndrome 58 9 0.010 None 1.000 1 1992 1992
Respiratory Distress Syndrome, Newborn
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases Disease or Syndrome 177 37 0.010 None 1.000 1 1992 1992
CUI: C0079293
Disease: Epidermolysis Bullosa Acquisita
Epidermolysis Bullosa Acquisita
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 32 0.010 None 1.000 1 1993 1993