Hypolipoproteinemias
|
phenotype |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Finding
|
1
|
|
0.300 |
None |
1.000 |
1 |
|
1999 |
1999 |
Retinal vascular occlusion
|
disease |
Eye Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Contagious bovine pleuropneumonia
|
disease |
Infections; Respiratory Tract Diseases
|
Disease or Syndrome
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
2015 |
2015 |
Cilioretinal artery occlusion
|
disease |
Eye Diseases; Nervous System Diseases; Cardiovascular Diseases
|
Acquired Abnormality
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
1998 |
1998 |
Hypoprebetalipoproteinemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
1
|
|
0.300 |
None |
1.000 |
1 |
|
1999 |
1999 |
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
|
|
|
Recurrent pulmonary embolism
|
disease |
Respiratory Tract Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
2002 |
2002 |
Refractory angina
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
3
|
1
|
0.020 |
None |
1.000 |
2 |
|
2017 |
2020 |
Calcific stenosis
|
disease |
Pathological Conditions, Signs and Symptoms
|
Acquired Abnormality
|
3
|
4
|
0.010 |
None |
1.000 |
1 |
1
|
2014 |
2014 |
Plasminogen Deficiency, Type I
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
3
|
13
|
0.010 |
None |
1.000 |
1 |
|
1998 |
1998 |
Perinatal stroke
|
disease |
|
Disease or Syndrome
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
Hepatic amyloidosis
|
disease |
Digestive System Diseases; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
4
|
|
0.010 |
None |
1.000 |
1 |
|
2003 |
2003 |
Logopenic progressive aphasia
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Mental or Behavioral Dysfunction
|
4
|
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
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 |
Heterozygous Factor V Leiden mutation
|
disease |
|
Disease or Syndrome
|
6
|
|
0.020 |
None |
1.000 |
2 |
|
2007 |
2011 |
response to statin
|
phenotype |
|
Organism Function
|
6
|
8
|
0.100 |
None |
1.000 |
1 |
1
|
2012 |
2012 |
Factor XIII deficiency disease
|
disease |
|
Disease or Syndrome
|
6
|
2
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
Primary hypercholesterolemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
7
|
2
|
0.020 |
None |
0.500 |
2 |
|
1992 |
2018 |
Central Retinal Artery Occlusion
|
disease |
Eye Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
7
|
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Rheumatic aortic stenosis
|
disease |
Infections; Cardiovascular Diseases
|
Disease or Syndrome
|
7
|
5
|
0.100 |
None |
1.000 |
1 |
1
|
2018 |
2018 |
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 |
Calcification of mitral valve
|
disease |
|
Disease or Syndrome
|
8
|
2
|
0.010 |
None |
1.000 |
1 |
1
|
2016 |
2016 |
Hypoplasminogenemia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
9
|
3
|
0.020 |
None |
1.000 |
2 |
|
1995 |
2020 |
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 |
Porencephaly
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
9
|
3
|
0.010 |
None |
1.000 |
1 |
|
1998 |
1998 |