SELPLG, selectin P ligand, 6404

N. diseases: 113; N. variants: 1
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: C0406549
Disease: Cutis laxa, acquired type
Cutis laxa, acquired type 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 3 0.010 None 1.000 1 2017 2017
CUI: C0563306
Disease: IgG myeloma
IgG myeloma 		disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Neoplastic Process 4 0.010 None 1.000 1 2017 2017
CUI: C0281902
Disease: maladjustment
maladjustment 		phenotype Mental or Behavioral Dysfunction 13 0.010 None 1.000 1 2017 2017
CUI: C3853962
Disease: Enterovirus 71 infection
Enterovirus 71 infection 		disease Infections Disease or Syndrome 21 2 0.020 None 1.000 2 2010 2012
CUI: C1136084
Disease: Plasma cell dyscrasia
Plasma cell dyscrasia 		disease Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 36 0.010 None 1.000 1 2017 2017
CUI: C0014742
Disease: Erythema Multiforme
Erythema Multiforme 		disease Skin and Connective Tissue Diseases Disease or Syndrome 38 2 0.010 None 1.000 1 2005 2005
CUI: C0085693
Disease: Acute appendicitis NOS (disorder)
Acute appendicitis NOS (disorder) 		disease Digestive System Diseases; Infections Disease or Syndrome 43 2 0.010 None 1.000 1 2017 2017
CUI: C1320214
Disease: Invasive Streptococcus pneumoniae disease
Invasive Streptococcus pneumoniae disease 		disease Infections Disease or Syndrome 55 9 0.010 None 1.000 1 2016 2016
CUI: C0234233
Disease: Sore to touch
Sore to touch 		phenotype Pathological Conditions, Signs and Symptoms; Mental Disorders Sign or Symptom 56 8 0.010 None 1.000 1 2019 2019
CUI: C0018572
Disease: Hand, Foot and Mouth Disease
Hand, Foot and Mouth Disease 		disease Infections Disease or Syndrome 63 13 0.010 None 1.000 1 2017 2017
CUI: C0003175
Disease: Anthrax disease
Anthrax disease 		disease Infections Disease or Syndrome 66 3 0.010 None 1.000 1 2017 2017
CUI: C0010495
Disease: Cutis Laxa
Cutis Laxa 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 70 21 0.010 None 1.000 1 2017 2017
CUI: C0003615
Disease: Appendicitis
Appendicitis 		disease Digestive System Diseases; Infections Disease or Syndrome 83 10 0.010 None 1.000 1 2017 2017
CUI: C0032269
Disease: Pneumococcal Infections
Pneumococcal Infections 		group Infections Disease or Syndrome 85 1 0.010 None 1.000 1 2016 2016
CUI: C0085278
Disease: Antiphospholipid Syndrome
Antiphospholipid Syndrome 		disease Immune System Diseases Disease or Syndrome 99 17 0.020 None 1.000 2 2007 2018
CUI: C0155862
Disease: Streptococcal pneumonia
Streptococcal pneumonia 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 100 2 0.010 None 1.000 1 2013 2013
CUI: C0010036
Disease: Corneal dystrophy
Corneal dystrophy 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 113 25 0.010 None 1.000 1 2020 2020
CUI: C0030805
Disease: Bullous pemphigoid
Bullous pemphigoid 		disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 127 11 0.010 None 1.000 1 2007 2007
CUI: C4551993
Disease: Amyotrophic Lateral Sclerosis, Familial
Amyotrophic Lateral Sclerosis, Familial 		disease Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 130 68 0.300 None 1.000 1 2002 2002
CUI: C0032300
Disease: Lobar Pneumonia
Lobar Pneumonia 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 140 2 0.010 None 1.000 1 2013 2013
CUI: C0019069
Disease: Hemophilia A
Hemophilia A 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 143 295 0.010 None 1.000 1 2003 2003
CUI: C0748355
Disease: Acute respiratory distress
Acute respiratory distress 		disease Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases Disease or Syndrome 147 6 0.010 None 1.000 1 2018 2018
CUI: C0398623
Disease: Thrombophilia
Thrombophilia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 161 43 0.010 None 1.000 1 2017 2017
CUI: C1862939
Disease: AMYOTROPHIC LATERAL SCLEROSIS 1
AMYOTROPHIC LATERAL SCLEROSIS 1 		disease Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 164 139 0.300 None 1.000 1 2002 2002
CUI: C0085409
Disease: Polyendocrinopathies, Autoimmune
Polyendocrinopathies, Autoimmune 		group Immune System Diseases; Endocrine System Diseases Disease or Syndrome 166 21 0.020 None 1.000 2 2007 2017