Source: BEFREE ×
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: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
phenotype Neoplastic Process 6626 169 0.100 None 1.000 13 2007 2019
CUI: C0544848
Disease: Dystrophy, granular
Dystrophy, granular
disease Disease or Syndrome 4 8 0.050 None 1.000 5 6 1995 2016
CUI: C2939149
Disease: Amyloid of cornea
Amyloid of cornea
disease Disease or Syndrome 4 5 0.040 None 0.750 4 3 2004 2007
CUI: C4700127
Disease: Thiel-behnke
Thiel-behnke
disease Disease or Syndrome 2 2 0.030 None 1.000 3 2 1999 2008
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
disease Disease or Syndrome 1075 276 0.020 None 1.000 2 1 2008 2009
CUI: C2347748
Disease: Adult Erythroleukemia
Adult Erythroleukemia
disease Neoplastic Process 236 4 0.020 None 1.000 2 1990 1991
CUI: C0026985
Disease: Myelodysplasia
Myelodysplasia
disease Congenital Abnormality 135 3 0.010 None 1.000 1 1994 1994
CUI: C0028259
Disease: Nodule
Nodule
phenotype Acquired Abnormality 278 19 0.010 None 1.000 1 2000 2000
CUI: C0268070
Disease: Hypocupremia
Hypocupremia
disease Disease or Syndrome 21 0.010 None 1.000 1 2019 2019
CUI: C0860659
Disease: Aloof
Aloof
disease Mental or Behavioral Dysfunction 81 0.010 None 1.000 1 1996 1996
CUI: C1402315
Disease: Vascular lesions
Vascular lesions
disease Disease or Syndrome 111 9 0.010 None 1.000 1 1996 1996
CUI: C1658953
Disease: tumor vasculature
tumor vasculature
phenotype Neoplastic Process 200 0.010 None 1.000 1 2013 2013
CUI: C2921627
Disease: Clinically isolated syndrome
Clinically isolated syndrome
disease Disease or Syndrome 54 2 0.010 None 1.000 1 2018 2018
CUI: C4699184
Disease: Fuchs
Fuchs
disease Disease or Syndrome 10 5 0.010 None 1.000 1 1996 1996
CUI: C4733095
Disease: HER2-negative breast cancer
HER2-negative breast cancer
disease Neoplastic Process 160 18 0.010 None 1.000 1 2019 2019
CUI: C0344315
Disease: Depressed mood
Depressed mood
phenotype Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 1459 269 0.010 None 1.000 1 2007 2007
CUI: C0018799
Disease: Heart Diseases
Heart Diseases
group Cardiovascular Diseases Disease or Syndrome 476 44 0.010 None 1.000 1 2017 2017
CUI: C0010036
Disease: Corneal dystrophy
Corneal dystrophy
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 44 20 0.200 None 0.992 117 7 1996 2019
CUI: C1690006
Disease: Lattice corneal dystrophy Type I
Lattice corneal dystrophy Type I
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 11 12 0.800 strong 0.960 45 10 1998 2019
CUI: C1275685
Disease: Avellino corneal dystrophy
Avellino corneal dystrophy
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 114 14 0.800 strong 1.000 38 5 1998 2019
CUI: C0018179
Disease: Granular Dystrophy, Corneal
Granular Dystrophy, Corneal
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 7 6 0.200 None 0.964 28 5 1994 2018
CUI: C0339278
Disease: Reis-Bucklers' corneal dystrophy
Reis-Bucklers' corneal dystrophy
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 2 6 0.800 strong 0.950 17 5 1998 2019
CUI: C1562894
Disease: Thiel-Behnke corneal dystrophy
Thiel-Behnke corneal dystrophy
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 12 4 0.750 strong 1.000 5 4 1998 2015
CUI: C0016781
Disease: Fuchs Endothelial Dystrophy
Fuchs Endothelial Dystrophy
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 90 25 0.040 None 1.000 4 1996 2019
Groenouw corneal dystrophy type I (disorder)
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 1 2 0.730 strong 1.000 3 2 1998 2011