APOB, apolipoprotein B, 338

N. diseases: 339; N. variants: 122
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: C0221253
Disease: Xanthoma tendinosum
Xanthoma tendinosum
disease Nutritional and Metabolic Diseases Disease or Syndrome 15 22 0.100 None 0
CUI: C0302314
Disease: Xanthoma
Xanthoma
disease Nutritional and Metabolic Diseases Disease or Syndrome 29 4 0.120 None 1.000 2 1982 1988
CUI: C1510471
Disease: Vitamin Deficiency
Vitamin Deficiency
group Nutritional and Metabolic Diseases Disease or Syndrome 17 2 0.010 None 1.000 1 2002 2002
CUI: C0042769
Disease: Virus Diseases
Virus Diseases
group Infections Disease or Syndrome 1471 42 0.040 None 1.000 4 2009 2017
CUI: C0242698
Disease: Ventricular Dysfunction, Left
Ventricular Dysfunction, Left
phenotype Cardiovascular Diseases Pathologic Function 88 0.100 None 0
CUI: C0042373
Disease: Vascular Diseases
Vascular Diseases
group Cardiovascular Diseases Disease or Syndrome 688 40 0.040 None 1.000 4 2004 2009
CUI: C0856738
Disease: Triple vessel disease
Triple vessel disease
disease Cardiovascular Diseases Disease or Syndrome 13 3 0.010 None < 0.001 1 1998 1998
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
phenotype Laboratory Procedure 563 1418 0.100 None 1.000 10 9 2007 2019
CUI: C0007787
Disease: Transient Ischemic Attack
Transient Ischemic Attack
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 344 16 0.010 None 1.000 1 2018 2018
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma
disease Neoplasms; Endocrine System Diseases Neoplastic Process 1175 145 0.010 None 1.000 1 2019 2019
CUI: C0398623
Disease: Thrombophilia
Thrombophilia
disease Hemic and Lymphatic Diseases Disease or Syndrome 161 43 0.010 None 1.000 1 2 2018 2018
CUI: C0836924
Disease: Thrombocytosis
Thrombocytosis
disease Hemic and Lymphatic Diseases Disease or Syndrome 93 12 0.010 None 1.000 1 2018 2018
CUI: C4476910
Disease: Thin-cap fibroatheroma
Thin-cap fibroatheroma
phenotype Cardiovascular Diseases Acquired Abnormality 12 0.010 None 1.000 1 2018 2018
CUI: C1963961
Disease: Testosterone deficiency
Testosterone deficiency
disease Disease or Syndrome 24 1 0.010 None 1.000 1 2006 2006
CUI: C0949664
Disease: Tauopathies
Tauopathies
group Nervous System Diseases Disease or Syndrome 245 43 0.010 None 1.000 1 2018 2018
CUI: C0039292
Disease: Tangier Disease
Tangier Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 31 28 0.020 None 1.000 2 1990 2001
CUI: C0003499
Disease: Supravalvular aortic stenosis
Supravalvular aortic stenosis
disease Cardiovascular Diseases Disease or Syndrome 23 38 0.100 None 0
CUI: C0085298
Disease: Sudden Cardiac Death
Sudden Cardiac Death
phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 133 40 0.100 None 0
CUI: C2711227
Disease: Steatohepatitis
Steatohepatitis
disease Digestive System Diseases Disease or Syndrome 1143 75 0.500 None 1.000 19 1996 2018
CUI: C0259771
Disease: Steatocystoma multiplex
Steatocystoma multiplex
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Neoplastic Process 3 4 0.010 None 1.000 1 1991 1991
CUI: C1318973
Disease: Staphylococcus aureus infection
Staphylococcus aureus infection
disease Infections Disease or Syndrome 49 4 0.010 None 1.000 1 2008 2008
CUI: C4525305
Disease: Stage IV Gallbladder Cancer AJCC v8
Stage IV Gallbladder Cancer AJCC v8
disease Neoplastic Process 367 56 0.030 None 1.000 3 2004 2013
Stage III Gallbladder Cancer AJCC v8
disease Neoplastic Process 367 56 0.030 None 1.000 3 2004 2013
Stage IIB Gallbladder Cancer AJCC v8
disease Neoplastic Process 367 56 0.030 None 1.000 3 2004 2013
Stage IIA Gallbladder Cancer AJCC v8
disease Neoplastic Process 367 56 0.030 None 1.000 3 2004 2013