CD36, CD36 molecule, 948

N. diseases: 351; N. variants: 61
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: C1332632
Disease: Breast Liposarcoma
Breast Liposarcoma 		disease Neoplasms Neoplastic Process 1 0.010 None 1.000 1 2011 2011
CUI: C1970441
Disease: CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 7
CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 7 		phenotype Finding 1 1 0.100 None 0 1
CUI: C0242147
Disease: Acute urinary tract infection
Acute urinary tract infection 		disease Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases Disease or Syndrome 3 0.010 None 1.000 1 2018 2018
CUI: C1832390
Disease: Van Maldergem Wetzburger Verloes syndrome
Van Maldergem Wetzburger Verloes syndrome 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Disease or Syndrome 4 0.010 None 1.000 1 2017 2017
CUI: C3547188
Disease: response to fenofibrate
response to fenofibrate 		phenotype Cell Function 4 5 0.100 None 1.000 1 1 2012 2012
CUI: C0339808
Disease: House dust mite allergy
House dust mite allergy 		phenotype Pathological Conditions, Signs and Symptoms; Infections; Immune System Diseases Disease or Syndrome 5 0.010 None 1.000 1 2017 2017
CUI: C1970028
Disease: MALARIA, SUSCEPTIBILITY TO (finding)
MALARIA, SUSCEPTIBILITY TO (finding) 		disease Finding 5 23 0.100 None 0 2
CUI: C0042875
Disease: Vitamin E Deficiency
Vitamin E Deficiency 		disease Nutritional and Metabolic Diseases Disease or Syndrome 6 0.010 None 1.000 1 2006 2006
CUI: C0340834
Disease: Hennekam lymphangiectasia-lymphedema syndrome
Hennekam lymphangiectasia-lymphedema syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 6 0.010 None 1.000 1 2017 2017
CUI: C0577698
Disease: Exercise-induced angina
Exercise-induced angina 		phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Sign or Symptom 7 5 0.010 None 1.000 1 1 2007 2007
CUI: C4025823
Disease: Abnormality of the endocrine system
Abnormality of the endocrine system 		disease Anatomical Abnormality 7 1 0.100 None 0
CUI: C2678045
Disease: TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS
TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital Diseases Disease or Syndrome; Congenital Abnormality 10 3 0.010 None 1.000 1 2019 2019
CUI: C0333864
Disease: Giant platelet (morphologic abnormality)
Giant platelet (morphologic abnormality) 		phenotype Finding 10 0.100 None 0
CUI: C2697501
Disease: Giant Platelet Count (procedure)
Giant Platelet Count (procedure) 		phenotype Laboratory Procedure 10 0.100 None 0
CUI: C4755296
Disease: Susceptibility to viral and mycobacterial infection
Susceptibility to viral and mycobacterial infection 		disease Disease or Syndrome 11 3 0.010 None 1.000 1 2007 2007
CUI: C0856151
Disease: Fat redistribution
Fat redistribution 		phenotype Disease or Syndrome 12 0.010 None 1.000 1 2016 2016
CUI: C3854603
Disease: FNAITP
FNAITP 		disease Disease or Syndrome 12 2 0.010 None 1.000 1 2018 2018
CUI: C1842090
Disease: Platelet Glycoprotein IV Deficiency
Platelet Glycoprotein IV Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 14 12 0.900 None 0.973 37 12 1993 2019
CUI: C0018813
Disease: Myocardial rupture
Myocardial rupture 		disease Cardiovascular Diseases Disease or Syndrome 14 0.010 None 1.000 1 2018 2018
CUI: C1863844
Disease: Adult-onset citrullinemia type 2
Adult-onset citrullinemia type 2 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 14 15 0.010 None 1.000 1 2015 2015
CUI: C0221028
Disease: Neonatal thrombocytopenia (disorder)
Neonatal thrombocytopenia (disorder) 		disease Hemic and Lymphatic Diseases; Cardiovascular Diseases Disease or Syndrome 15 2 0.010 None 1.000 1 2002 2002
CUI: C4054325
Disease: Obesity Related Glomerulopathy
Obesity Related Glomerulopathy 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 16 0.020 None 1.000 2 2019 2019
CUI: C4022459
Disease: Decreased adipose tissue
Decreased adipose tissue 		phenotype Sign or Symptom 17 0.010 None 1.000 1 2019 2019
CUI: C0003257
Disease: Antibody Deficiency Syndrome
Antibody Deficiency Syndrome 		disease Immune System Diseases Disease or Syndrome 21 0.300 None 1.000 1 2005 2005
CUI: C1399793
Disease: skin fold (abnormality)
skin fold (abnormality) 		disease Anatomical Abnormality 21 8 0.010 None 1.000 1 1997 1997