APOC2, apolipoprotein C2, 344

N. diseases: 68; N. variants: 14
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: C0023462
Disease: Acute Megakaryocytic Leukemias
Acute Megakaryocytic Leukemias 		disease Neoplasms Neoplastic Process 159 15 0.010 None 1.000 1 2014 2014
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis 		disease Digestive System Diseases Disease or Syndrome 435 51 0.010 None 1.000 1 2018 2018
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		disease Nervous System Diseases; Mental Disorders Disease or Syndrome 3397 1843 0.140 None 0.800 5 1 1987 2018
CUI: C0002726
Disease: Amyloidosis
Amyloidosis 		disease Nutritional and Metabolic Diseases Disease or Syndrome 694 93 0.300 strong 1.000 1 2017 2017
CUI: C4017139
Disease: APOLIPOPROTEIN C-II (AUCKLAND) PHENOTYPE
APOLIPOPROTEIN C-II (AUCKLAND) PHENOTYPE 		phenotype Finding 2 1 0.100 None 0 1
CUI: C4017135
Disease: APOLIPOPROTEIN C-II (BARI) PHENOTYPE
APOLIPOPROTEIN C-II (BARI) PHENOTYPE 		phenotype Finding 2 1 0.100 None 0 1
CUI: C3889891
Disease: APOLIPOPROTEIN C-II (PADOVA) PHENOTYPE
APOLIPOPROTEIN C-II (PADOVA) PHENOTYPE 		phenotype Finding 2 1 0.100 None 0 1
CUI: C4017134
Disease: APOLIPOPROTEIN C-II (PARIS) PHENOTYPE
APOLIPOPROTEIN C-II (PARIS) PHENOTYPE 		phenotype Finding 2 1 0.100 None 0 1
CUI: C4017137
Disease: APOLIPOPROTEIN C-II (SAN FRANCISCO)
APOLIPOPROTEIN C-II (SAN FRANCISCO) 		phenotype Finding 2 1 0.100 None 0 1
CUI: C4017138
Disease: apolipoprotein C-II (Wakayama) phenotype
apolipoprotein C-II (Wakayama) phenotype 		phenotype Finding 2 1 0.100 None 0 1
CUI: C1720779
Disease: Apolipoprotein C-II Deficiency (disorder)
Apolipoprotein C-II Deficiency (disorder) 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 3 5 0.750 None 1.000 9 5 1993 2017
CUI: C4017136
Disease: APOLIPOPROTEIN C-II VARIANT PHENOTYPE
APOLIPOPROTEIN C-II VARIANT PHENOTYPE 		phenotype Finding 2 1 0.100 None 0 1
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		disease Cardiovascular Diseases Disease or Syndrome 2006 267 0.010 None 1.000 1 2001 2001
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		disease Cardiovascular Diseases Disease or Syndrome 2044 281 0.010 None 1.000 1 2001 2001
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		phenotype Laboratory Procedure 1156 2575 0.100 None 1.000 1 2 2018 2018
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		group Cardiovascular Diseases Disease or Syndrome 1756 711 0.020 None 1.000 2 2012 2018
CUI: C1274228
Disease: Chylomicronemia syndrome
Chylomicronemia syndrome 		disease Disease or Syndrome 2 0.010 None 1.000 1 2013 2013
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
Complete Trisomy 21 Syndrome 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 669 77 0.010 None 1.000 1 2014 2014
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		disease Cardiovascular Diseases Disease or Syndrome 1576 1178 0.010 None 1.000 1 1 2010 2010
CUI: C1291447
Disease: Deficiency of triacylglycerol lipase
Deficiency of triacylglycerol lipase 		disease Disease or Syndrome 3 0.010 None 1.000 1 1988 1988
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		disease Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 3134 2672 0.010 None < 0.001 1 1996 1996
CUI: C0013080
Disease: Down Syndrome
Down Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 766 80 0.010 None 1.000 1 2014 2014
CUI: C0011609
Disease: Drug Eruptions
Drug Eruptions 		group Skin and Connective Tissue Diseases; Immune System Diseases; Chemically-Induced Disorders Disease or Syndrome 41 0.300 None 1.000 1 2010 2010
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias 		group Nutritional and Metabolic Diseases Disease or Syndrome 471 184 0.030 None 0.667 3 1994 2017
CUI: C0221252
Disease: Eruptive xanthoma
Eruptive xanthoma 		disease Nutritional and Metabolic Diseases Disease or Syndrome 4 1 0.100 None 0