SELP, selectin P, 6403

N. diseases: 293; N. variants: 23
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: C0151947
Disease: Pulmonary artery thrombosis
Pulmonary artery thrombosis
disease Cardiovascular Diseases Disease or Syndrome 1 0.010 None 1.000 1 2019 2019
CUI: C0152172
Disease: Angina decubitus
Angina decubitus
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 1 0.010 None 1.000 1 2011 2011
CUI: C0334368
Disease: Mucin-producing adenocarcinoma
Mucin-producing adenocarcinoma
disease Neoplasms Neoplastic Process 1 0.010 None 1.000 1 1998 1998
CUI: C3890352
Disease: P-Selectin Measurement
P-Selectin Measurement
phenotype Laboratory Procedure 1 2 0.100 None 1.000 1 1 2017 2017
CUI: C4050627
Disease: Soluble P-Selectin Measurement
Soluble P-Selectin Measurement
phenotype Laboratory Procedure 1 3 0.100 None 1.000 1 2 2010 2010
CUI: C0019021
Disease: Hemoglobin C Disease
Hemoglobin C Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 3 0.010 None < 0.001 1 2008 2008
Thrombocytopenia due to sequestration
disease Hemic and Lymphatic Diseases Disease or Syndrome 5 0.010 None 1.000 1 2018 2018
Diarrhea-associated hemolytic uremic syndrome
disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 5 0.010 None 1.000 1 2011 2011
CUI: C4049381
Disease: Cancer-associated thrombosis
Cancer-associated thrombosis
disease Disease or Syndrome 10 0.010 None 1.000 1 2017 2017
CUI: C0012359
Disease: Pathological Dilatation
Pathological Dilatation
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 11 0.010 None 1.000 1 2007 2007
CUI: C1264041
Disease: von Willebrand Disease, Type 3
von Willebrand Disease, Type 3
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 11 17 0.010 None 1.000 1 2005 2005
CUI: C4728213
Disease: PIK3CA related overgrowth spectrum
PIK3CA related overgrowth spectrum
disease Disease or Syndrome 11 9 0.010 None 1.000 1 2019 2019
CUI: C0262469
Disease: Embolic stroke
Embolic stroke
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 13 2 0.010 None 1.000 1 1 2004 2004
CUI: C0311276
Disease: Severe malnutrition
Severe malnutrition
disease Disease or Syndrome 13 1 0.010 None 1.000 1 2019 2019
CUI: C0265808
Disease: Cyanotic congenital heart disease
Cyanotic congenital heart disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Respiratory Tract Diseases; Cardiovascular Diseases Disease or Syndrome 14 0.010 None 1.000 1 2001 2001
CUI: C0746306
Disease: lupus cutaneous
lupus cutaneous
disease Disease or Syndrome 16 1 0.010 None 1.000 1 2017 2017
CUI: C0085261
Disease: Proteus Syndrome
Proteus Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases Neoplastic Process 17 1 0.010 None 1.000 1 2019 2019
CUI: C0009443
Disease: Common Cold
Common Cold
disease Infections; Respiratory Tract Diseases Disease or Syndrome 24 0.010 None 1.000 1 2007 2007
CUI: C0393576
Disease: Chorea Acanthocytosis Syndrome
Chorea Acanthocytosis Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 29 5 0.010 None 1.000 1 2013 2013
CUI: C0750151
Disease: Vaso-Occlusive Crisis
Vaso-Occlusive Crisis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 30 5 0.020 None 1.000 2 2017 2019
CUI: C1096458
Disease: Vascular occlusion
Vascular occlusion
disease Cardiovascular Diseases Disease or Syndrome 30 2 0.010 None 1.000 1 2006 2006
CUI: C0524702
Disease: Pulmonary Thromboembolisms
Pulmonary Thromboembolisms
disease Respiratory Tract Diseases; Cardiovascular Diseases Disease or Syndrome 33 6 0.010 None 1.000 1 2018 2018
CUI: C0235574
Disease: Intravascular hemolysis
Intravascular hemolysis
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 36 0.010 None 1.000 1 2019 2019
CUI: C0272302
Disease: Gray Platelet Syndrome
Gray Platelet Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 38 14 0.010 None 1.000 1 2017 2017
Anti-Basement Membrane Glomerulonephritis
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 39 0.200 None 1.000 1 2011 2011