Lp(A) Deficiency, Congenital
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
1
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
Cholesteryl Ester Transfer Protein Deficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
22
|
5
|
0.010 |
None |
1.000 |
1 |
|
1989 |
1989 |
Thrombophilia, hereditary
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
17
|
9
|
0.010 |
None |
1.000 |
1 |
|
1992 |
1992 |
Myocardial infarction, stroke
|
disease |
|
Disease or Syndrome
|
46
|
3
|
0.010 |
None |
1.000 |
1 |
|
1992 |
1992 |
Familial hyperalphalipoproteinemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
5
|
|
0.010 |
None |
1.000 |
1 |
|
1993 |
1993 |
Glucocorticoid-remediable aldosteronism
|
disease |
Endocrine System Diseases
|
Disease or Syndrome
|
30
|
2
|
0.010 |
None |
1.000 |
1 |
|
1993 |
1993 |
Heart Diseases
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
537
|
45
|
0.030 |
None |
1.000 |
3 |
|
1992 |
1994 |
Hypoalphalipoproteinemia, Familial
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
18
|
6
|
0.020 |
None |
0.500 |
2 |
|
1994 |
1994 |
obsolete Combined hyperlipidemia
|
disease |
|
Disease or Syndrome
|
17
|
4
|
0.010 |
None |
1.000 |
1 |
|
1994 |
1994 |
Hyperkeratosis lenticularis perstans
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
18
|
11
|
0.010 |
None |
1.000 |
1 |
|
1994 |
1994 |
Familial hypobetalipoproteinemia
|
disease |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
12
|
24
|
0.010 |
None |
< 0.001 |
1 |
|
1995 |
1995 |
Blood Coagulation Disorders
|
group |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
267
|
31
|
0.010 |
None |
1.000 |
1 |
|
1995 |
1995 |
Hypobetalipoproteinemias
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
20
|
11
|
0.010 |
None |
< 0.001 |
1 |
|
1995 |
1995 |
Hyperthyroidism
|
disease |
Endocrine System Diseases
|
Disease or Syndrome
|
279
|
27
|
0.010 |
None |
1.000 |
1 |
|
1995 |
1995 |
Primary biliary cirrhosis
|
disease |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
|
Disease or Syndrome
|
478
|
667
|
0.010 |
None |
1.000 |
1 |
|
1996 |
1996 |
Liver neoplasms
|
group |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
1424
|
7
|
0.010 |
None |
1.000 |
1 |
|
1996 |
1996 |
Thromboembolism
|
phenotype |
Cardiovascular Diseases
|
Pathologic Function
|
25
|
3
|
0.500 |
None |
1.000 |
1 |
|
1997 |
1997 |
Cooley's anemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
144
|
19
|
0.010 |
None |
1.000 |
1 |
|
1997 |
1997 |
IGA Glomerulonephritis
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases
|
Disease or Syndrome
|
456
|
130
|
0.010 |
None |
1.000 |
1 |
|
1997 |
1997 |
Hypoalphalipoproteinemias
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
20
|
7
|
0.010 |
None |
1.000 |
1 |
|
1997 |
1997 |
Venous Thrombosis
|
phenotype |
Cardiovascular Diseases
|
Pathologic Function
|
117
|
218
|
0.300 |
None |
1.000 |
1 |
|
1997 |
1997 |
Zellweger Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nervous System Diseases
|
Disease or Syndrome
|
36
|
1
|
0.010 |
None |
1.000 |
1 |
|
1997 |
1997 |
Peroxisomal Disorders
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
25
|
1
|
0.010 |
None |
1.000 |
1 |
|
1997 |
1997 |
Chondrodysplasia Punctata, Rhizomelic
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
|
Disease or Syndrome
|
8
|
1
|
0.010 |
None |
< 0.001 |
1 |
|
1997 |
1997 |
Congenital porencephaly
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Congenital Abnormality
|
9
|
3
|
0.010 |
None |
1.000 |
1 |
|
1998 |
1998 |