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: C4017139
Disease: APOLIPOPROTEIN C-II (AUCKLAND) PHENOTYPE
APOLIPOPROTEIN C-II (AUCKLAND) 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: C0019209
Disease: Hepatomegaly
Hepatomegaly 		phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Finding 523 30 0.100 None 0
CUI: C0339477
Disease: Lipidemia retinalis
Lipidemia retinalis 		disease Eye Diseases Disease or Syndrome 4 0.100 None 0
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: C4017138
Disease: apolipoprotein C-II (Wakayama) phenotype
apolipoprotein C-II (Wakayama) 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: C4017135
Disease: APOLIPOPROTEIN C-II (BARI) PHENOTYPE
APOLIPOPROTEIN C-II (BARI) PHENOTYPE 		phenotype Finding 2 1 0.100 None 0 1
CUI: C4017136
Disease: APOLIPOPROTEIN C-II VARIANT PHENOTYPE
APOLIPOPROTEIN C-II VARIANT PHENOTYPE 		phenotype Finding 2 1 0.100 None 0 1
CUI: C0268199
Disease: Familial apolipoprotein C-II deficiency
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: 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
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: C2239176
Disease: Liver carcinoma
Liver carcinoma 		disease Digestive System Diseases; Neoplasms Neoplastic Process 5725 942 0.010 None 1.000 1 1985 1985
CUI: C0302314
Disease: Xanthoma
Xanthoma 		disease Nutritional and Metabolic Diseases Disease or Syndrome 29 4 0.010 None 1.000 1 1986 1986
CUI: C0043325
Disease: Xanthomatosis
Xanthomatosis 		disease Nutritional and Metabolic Diseases Disease or Syndrome 20 10 0.010 None 1.000 1 1986 1986
CUI: C0162429
Disease: Malnutrition
Malnutrition 		disease Nutritional and Metabolic Diseases Disease or Syndrome 417 29 0.010 None 1.000 1 1986 1986
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: C0020479
Disease: Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type III 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 28 24 0.010 None 1.000 1 1988 1988
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: C3250443
Disease: MYOTONIC DYSTROPHY 1
MYOTONIC DYSTROPHY 1 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 179 14 0.020 None 1.000 2 1990 1991
CUI: C0020597
Disease: Hypobetalipoproteinemias
Hypobetalipoproteinemias 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 20 11 0.010 None 1.000 1 1991 1991
CUI: C1862596
Disease: Familial hypobetalipoproteinemia
Familial hypobetalipoproteinemia 		disease Nutritional and Metabolic Diseases Disease or Syndrome 12 24 0.010 None 1.000 1 1991 1991
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		phenotype Nutritional and Metabolic Diseases Disease or Syndrome 340 169 0.200 None 0.960 25 1 1992 2019