FZD4, frizzled class receptor 4, 8322

N. diseases: 239; N. variants: 28
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.
Familial Exudative Vitreoretinopathy
disease Congenital Abnormality 19 18 0.200 None 1.000 49 7 2000 2019
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
phenotype Neoplastic Process 6626 169 0.100 None 1.000 10 2012 2019
CUI: C0344290
Disease: Vitreoretinal degeneration
Vitreoretinal degeneration
disease Disease or Syndrome 20 6 0.030 None 1.000 3 2003 2015
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
disease Disease or Syndrome 1075 276 0.020 None 1.000 2 2003 2005
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction
phenotype Disease or Syndrome 716 25 0.010 None 1.000 1 2019 2019
CUI: C0857116
Disease: Gross obesity
Gross obesity
disease Disease or Syndrome 12 0.010 None 1.000 1 2018 2018
CUI: C0858600
Disease: Taste sweet
Taste sweet
phenotype Sign or Symptom 41 3 0.010 None 1.000 1 2018 2018
CUI: C0877008
Disease: Enzyme inhibition disorder
Enzyme inhibition disorder
phenotype Disease or Syndrome 171 1 0.010 None 1.000 1 2018 2018
CUI: C1334386
Disease: Meningeal melanoma
Meningeal melanoma
disease Neoplastic Process 23 1 0.010 None 1.000 1 2019 2019
Differentiated Thyroid Gland Carcinoma
disease Neoplastic Process 245 80 0.010 None 1.000 1 2019 2019
Human immunodeficiency virus (HIV) II infection category B1
disease Disease or Syndrome 985 56 0.010 None 1.000 1 1997 1997
CUI: C4072980
Disease: Exudative vitreoretinopathy
Exudative vitreoretinopathy
disease Disease or Syndrome 6 2 0.110 None 1.000 1 2006 2006
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease
disease Disease or Syndrome 741 81 0.010 None 1.000 1 2018 2018
Malignant neoplasm of colon and/or rectum
disease Neoplastic Process 3669 502 0.010 None 1.000 1 2018 2018
Primary differentiated carcinoma of thyroid gland
disease Neoplastic Process 167 41 0.010 None 1.000 1 2019 2019
CUI: C0240897
Disease: Retinal exudates
Retinal exudates
phenotype Finding 5 1 0.100 None 0
CUI: C0344550
Disease: Congenital retinal fold
Congenital retinal fold
disease Congenital Abnormality 3 0.100 None 0
CUI: C1843517
Disease: Retinal arteriolar tortuosity
Retinal arteriolar tortuosity
phenotype Finding 23 0.100 None 0
CUI: C1851406
Disease: Peripheral retinal avascularization
Peripheral retinal avascularization
phenotype Finding 2 0.100 None 0
CUI: C1854494
Disease: Slow progression
Slow progression
phenotype Finding 165 0.100 None 0
EXUDATIVE VITREORETINOPATHY, DIGENIC
disease Finding 2 1 0.100 None 0 1
CUI: C3805574
Disease: Increased fracture rate
Increased fracture rate
phenotype Finding 123 0.100 None 0
CUI: C0011570
Disease: Mental Depression
Mental Depression
disease Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 1478 271 0.010 None 1.000 1 2011 2011
CUI: C0020175
Disease: Hunger
Hunger
phenotype Behavior and Behavior Mechanisms Sign or Symptom 70 12 0.010 None 1.000 1 2019 2019
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
phenotype Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 910 121 0.010 None 1.000 1 2009 2009