Apolipoprotein C-II Deficiency (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
2
|
|
0.750 |
None |
1.000 |
5 |
|
1993 |
2017 |
Hyperlipoproteinemia Type I
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
36
|
26
|
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 |
3 |
|
1979 |
2018 |
Hypertriglyceridemia
|
phenotype |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
266
|
155
|
0.200 |
None |
0.960 |
24 |
1
|
1992 |
2019 |
Pancreatitis
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
359
|
66
|
0.160 |
None |
1.000 |
6 |
|
1998 |
2020 |
Alzheimer's Disease
|
disease |
Nervous System Diseases; Mental Disorders
|
Disease or Syndrome
|
3131
|
968
|
0.140 |
None |
0.800 |
4 |
|
1987 |
2018 |
Myotonic Dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
154
|
4
|
0.100 |
None |
1.000 |
23 |
|
1985 |
2007 |
Pancreatitis, Chronic
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
362
|
54
|
0.040 |
None |
1.000 |
4 |
|
2006 |
2017 |
Dyslipidemias
|
group |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
460
|
184
|
0.030 |
None |
0.667 |
3 |
|
1994 |
2017 |
Recurrent pancreatitis
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
10
|
12
|
0.030 |
None |
1.000 |
3 |
|
2006 |
2017 |
Neoplasms
|
group |
Neoplasms
|
Neoplastic Process
|
10153
|
1571
|
0.020 |
None |
1.000 |
2 |
|
1994 |
2015 |
MYOTONIC DYSTROPHY 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
179
|
12
|
0.020 |
None |
1.000 |
2 |
|
1990 |
1991 |
Cardiovascular Diseases
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
1551
|
382
|
0.020 |
None |
1.000 |
2 |
|
2012 |
2018 |
Hyperlipidemia
|
disease |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
424
|
83
|
0.020 |
None |
1.000 |
2 |
|
2007 |
2015 |
Multiple Sclerosis
|
disease |
Immune System Diseases; Nervous System Diseases
|
Disease or Syndrome
|
1599
|
448
|
0.020 |
None |
1.000 |
2 |
|
1999 |
2018 |
Hypoalphalipoproteinemias
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
20
|
7
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Xanthoma
|
disease |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
21
|
4
|
0.010 |
None |
1.000 |
1 |
|
1986 |
1986 |
Impaired glucose tolerance
|
phenotype |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
555
|
80
|
0.010 |
None |
< 0.001 |
1 |
|
1996 |
1996 |
Mild cognitive disorder
|
disease |
Mental Disorders
|
Mental or Behavioral Dysfunction
|
427
|
94
|
0.010 |
None |
1.000 |
1 |
|
2011 |
2011 |
Hyperlipoproteinemia Type IIa
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
198
|
139
|
0.010 |
None |
1.000 |
1 |
|
1993 |
1993 |
Chylomicronemia syndrome
|
disease |
|
Disease or Syndrome
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
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 |
Multiple Chronic Conditions
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
929
|
42
|
0.010 |
None |
1.000 |
1 |
|
2004 |
2004 |
Plaque, Amyloid
|
disease |
Pathological Conditions, Signs and Symptoms
|
Acquired Abnormality
|
122
|
10
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Familial hyperchylomicronemia syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
5
|
2
|
0.010 |
None |
1.000 |
1 |
|
2014 |
2014 |