Early-onset coronary artery disease
|
phenotype |
|
Finding
|
1
|
2
|
0.100 |
None |
1.000 |
2 |
2
|
2011 |
2013 |
Pinguecula
|
disease |
Eye Diseases
|
Disease or Syndrome
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
2004 |
2004 |
Atypical angina
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
2
|
0.010 |
None |
1.000 |
1 |
2
|
2008 |
2008 |
Secondary hyperlipidemia
|
phenotype |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
1
|
|
0.010 |
None |
< 0.001 |
1 |
|
2001 |
2001 |
Familial hypercholesterolemia due to genetic defect of apolipoprotein B
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Bone xanthoma
|
disease |
Musculoskeletal Diseases
|
Disease or Syndrome
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
2015 |
2015 |
Retrosternal pain
|
phenotype |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Sign or Symptom
|
2
|
7
|
0.010 |
None |
1.000 |
1 |
3
|
1998 |
1998 |
Hypercholesterolemia result
|
phenotype |
|
Finding
|
3
|
415
|
0.100 |
None |
1.000 |
2 |
413
|
1992 |
1992 |
lipoprotein disorder
|
disease |
Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
1999 |
1999 |
Dissection of carotid artery
|
disease |
Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
3
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
Carotid Artery, Internal, Dissection
|
disease |
Nervous System Diseases; Cardiovascular Diseases; Wounds and Injuries
|
Disease or Syndrome
|
4
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
LIPOPROTEIN GLOMERULOPATHY
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
5
|
3
|
0.020 |
None |
1.000 |
2 |
|
2001 |
2018 |
Adiponectin Deficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
5
|
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
HEPATIC LIPASE DEFICIENCY (disorder)
|
disease |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
5
|
4
|
0.010 |
None |
1.000 |
1 |
|
2008 |
2008 |
HMG CoA lyase deficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
6
|
29
|
0.010 |
None |
1.000 |
1 |
|
2008 |
2008 |
Coxiella burnetii Infection
|
disease |
Infections
|
Disease or Syndrome
|
6
|
|
0.300 |
None |
1.000 |
1 |
|
2006 |
2006 |
Abnormality of nervous system physiology
|
phenotype |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Pathologic Function
|
6
|
|
0.100 |
None |
|
0 |
|
|
|
Abnormal eye physiology
|
phenotype |
|
Pathologic Function
|
6
|
|
0.100 |
None |
|
0 |
|
|
|
Cerebral artery atherosclerosis
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
6
|
|
0.100 |
None |
|
0 |
|
|
|
Myocardial steatosis
|
phenotype |
|
Finding
|
6
|
|
0.100 |
None |
|
0 |
|
|
|
Primary hypercholesterolemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
7
|
2
|
0.040 |
None |
1.000 |
4 |
1
|
1998 |
2014 |
Abnormal internal carotid artery morphology
|
disease |
|
Finding
|
7
|
|
0.100 |
None |
|
0 |
|
|
|
NIEMANN-PICK DISEASE, TYPE C2
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
9
|
22
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Premature arteriosclerosis
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
9
|
|
0.100 |
None |
|
0 |
|
|
|
Precocious atherosclerosis
|
phenotype |
Cardiovascular Diseases
|
Pathologic Function
|
9
|
|
0.100 |
None |
|
0 |
|
|
|