LPA, lipoprotein(a), 4018

N. diseases: 340; N. variants: 49
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: C0020623
Disease: Hypolipoproteinemias
Hypolipoproteinemias 		phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Finding 1 0.300 None 1.000 1 1999 1999
CUI: C0035326
Disease: Retinal vascular occlusion
Retinal vascular occlusion 		disease Eye Diseases; Cardiovascular Diseases Disease or Syndrome 1 0.010 None 1.000 1 2013 2013
CUI: C0276044
Disease: Contagious bovine pleuropneumonia
Contagious bovine pleuropneumonia 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 1 0.010 None 1.000 1 2015 2015
CUI: C0339495
Disease: Cilioretinal artery occlusion
Cilioretinal artery occlusion 		disease Eye Diseases; Nervous System Diseases; Cardiovascular Diseases Acquired Abnormality 1 0.010 None 1.000 1 1998 1998
CUI: C1720772
Disease: Hypoprebetalipoproteinemia
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
CUI: C1835362
Disease: Lp(A) Deficiency, Congenital
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
CUI: C1735914
Disease: Recurrent pulmonary embolism
Recurrent pulmonary embolism 		disease Respiratory Tract Diseases; Cardiovascular Diseases Disease or Syndrome 2 0.010 None 1.000 1 2002 2002
CUI: C0741032
Disease: Refractory angina
Refractory angina 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 3 1 0.020 None 1.000 2 2017 2020
CUI: C0333184
Disease: Calcific stenosis
Calcific stenosis 		disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 3 4 0.010 None 1.000 1 1 2014 2014
CUI: C1968804
Disease: Plasminogen Deficiency, Type I
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
CUI: C3665816
Disease: Perinatal stroke
Perinatal stroke 		disease Disease or Syndrome 3 0.010 None 1.000 1 2007 2007
CUI: C0267839
Disease: Hepatic amyloidosis
Hepatic amyloidosis 		disease Digestive System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome 4 0.010 None 1.000 1 2003 2003
CUI: C4274665
Disease: Logopenic progressive aphasia
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
CUI: C3875011
Disease: Familial hyperalphalipoproteinemia
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
CUI: C0584984
Disease: Heterozygous Factor V Leiden mutation
Heterozygous Factor V Leiden mutation 		disease Disease or Syndrome 6 0.020 None 1.000 2 2007 2011
CUI: C3549252
Disease: response to statin
response to statin 		phenotype Organism Function 6 8 0.100 None 1.000 1 1 2012 2012
CUI: C4316906
Disease: Factor XIII deficiency disease
Factor XIII deficiency disease 		disease Disease or Syndrome 6 2 0.010 None 1.000 1 2007 2007
CUI: C0342879
Disease: Primary hypercholesterolemia
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
CUI: C0007688
Disease: Central Retinal Artery Occlusion
Central Retinal Artery Occlusion 		disease Eye Diseases; Cardiovascular Diseases Disease or Syndrome 7 0.010 None 1.000 1 2013 2013
CUI: C0155567
Disease: Rheumatic aortic stenosis
Rheumatic aortic stenosis 		disease Infections; Cardiovascular Diseases Disease or Syndrome 7 5 0.100 None 1.000 1 1 2018 2018
CUI: C0282529
Disease: Chondrodysplasia Punctata, Rhizomelic
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
CUI: C0919718
Disease: Calcification of mitral valve
Calcification of mitral valve 		disease Disease or Syndrome 8 2 0.010 None 1.000 1 1 2016 2016
CUI: C0398621
Disease: Hypoplasminogenemia
Hypoplasminogenemia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 9 3 0.020 None 1.000 2 1995 2020
CUI: C0302892
Disease: Congenital porencephaly
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
CUI: C4082173
Disease: Porencephaly
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