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.
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: C0023817
Disease: Hyperlipoproteinemia Type I
Hyperlipoproteinemia Type I
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 36 64 0.400 None 1.000 11 1981 2018
Familial apolipoprotein C-II deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 3 0.330 None 1.000 4 1979 2018
CUI: C0019208
Disease: Hepatoma, Novikoff
Hepatoma, Novikoff
disease Digestive System Diseases; Neoplasms Neoplastic Process; Experimental Model of Disease 125 0.300 None 1.000 1 2001 2001
CUI: C0019207
Disease: Hepatoma, Morris
Hepatoma, Morris
disease Digestive System Diseases; Neoplasms Neoplastic Process; Experimental Model of Disease 124 0.300 None 1.000 1 2001 2001
CUI: C0023904
Disease: Liver Neoplasms, Experimental
Liver Neoplasms, Experimental
phenotype Digestive System Diseases; Neoplasms Neoplastic Process; Experimental Model of Disease 152 0.300 None 1.000 1 2001 2001
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: C0406537
Disease: Morbilliform Drug Reaction
Morbilliform Drug Reaction
disease Skin and Connective Tissue Diseases; Immune System Diseases; Chemically-Induced Disorders Disease or Syndrome 24 0.300 None 1.000 1 2010 2010
CUI: C0086404
Disease: Experimental Hepatoma
Experimental Hepatoma
disease Digestive System Diseases; Neoplasms Neoplastic Process; Experimental Model of Disease 117 0.300 None 1.000 1 2001 2001
CUI: C0002726
Disease: Amyloidosis
Amyloidosis
disease Nutritional and Metabolic Diseases Disease or Syndrome 694 93 0.300 strong 1.000 1 2017 2017
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
phenotype Nutritional and Metabolic Diseases Disease or Syndrome 340 169 0.200 None 0.960 25 1 1992 2019
CUI: C0030305
Disease: Pancreatitis
Pancreatitis
disease Digestive System Diseases Disease or Syndrome 502 80 0.160 None 1.000 6 1998 2020
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: C0027126
Disease: Myotonic Dystrophy
Myotonic Dystrophy
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 155 4 0.100 None 1.000 23 1985 2007
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
phenotype Laboratory Procedure 1156 2575 0.100 None 1.000 1 2 2018 2018
CUI: C0339477
Disease: Lipidemia retinalis
Lipidemia retinalis
disease Eye Diseases Disease or Syndrome 4 0.100 None 0
APOLIPOPROTEIN C-II VARIANT PHENOTYPE
phenotype Finding 2 1 0.100 None 0 1
CUI: C0038002
Disease: Splenomegaly
Splenomegaly
phenotype Pathological Conditions, Signs and Symptoms Finding 345 19 0.100 None 0
CUI: C0221252
Disease: Eruptive xanthoma
Eruptive xanthoma
disease Nutritional and Metabolic Diseases Disease or Syndrome 4 1 0.100 None 0
CUI: C4017137
Disease: APOLIPOPROTEIN C-II (SAN FRANCISCO)
APOLIPOPROTEIN C-II (SAN FRANCISCO)
phenotype Finding 2 1 0.100 None 0 1
APOLIPOPROTEIN C-II (BARI) PHENOTYPE
phenotype Finding 2 1 0.100 None 0 1
APOLIPOPROTEIN C-II (PADOVA) PHENOTYPE
phenotype Finding 2 1 0.100 None 0 1
APOLIPOPROTEIN C-II (PARIS) PHENOTYPE
phenotype Finding 2 1 0.100 None 0 1
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly
phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Finding 523 30 0.100 None 0
apolipoprotein C-II (Wakayama) phenotype
phenotype Finding 2 1 0.100 None 0 1