ICAM1, intercellular adhesion molecule 1, 3383

N. diseases: 737; N. variants: 18
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: C2919576
Disease: Left sided ulcerative colitis
Left sided ulcerative colitis 		disease Digestive System Diseases Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C1855457
Disease: MALARIA, CEREBRAL, SUSCEPTIBILITY TO (finding)
MALARIA, CEREBRAL, SUSCEPTIBILITY TO (finding) 		disease Finding 1 1 0.100 None 0 1
CUI: C0014736
Disease: Erysipelothrix infection
Erysipelothrix infection 		disease Infections; Animal Diseases Disease or Syndrome 2 0.010 None 1.000 1 1994 1994
CUI: C0025427
Disease: Mercury Poisoning
Mercury Poisoning 		disease Chemically-Induced Disorders Injury or Poisoning 3 0.200 None 1.000 1 2010 2010
CUI: C0025472
Disease: Mesenteric Vascular Occlusion
Mesenteric Vascular Occlusion 		disease Digestive System Diseases; Cardiovascular Diseases Disease or Syndrome 3 0.200 None 1.000 1 1994 1994
CUI: C2937222
Disease: Chronic ulcerative proctitis
Chronic ulcerative proctitis 		disease Digestive System Diseases Disease or Syndrome 3 0.010 None 1.000 1 2018 2018
CUI: C0263222
Disease: Chronic eczema
Chronic eczema 		disease Skin and Connective Tissue Diseases Disease or Syndrome 4 0.010 None 1.000 1 2019 2019
CUI: C2609079
Disease: Mirror syndrome
Mirror syndrome 		disease Disease or Syndrome 4 0.010 None 1.000 1 2020 2020
CUI: C0948031
Disease: Primary Graft Dysfunction
Primary Graft Dysfunction 		phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 5 0.210 None 1.000 3 2000 2012
CUI: C0006110
Disease: Brain Death
Brain Death 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Pathologic Function 5 0.200 None 1.000 1 2010 2010
CUI: C0391820
Disease: Gouty nephropathy
Gouty nephropathy 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases Disease or Syndrome 5 0.010 None 1.000 1 2020 2020
CUI: C0005750
Disease: Blind Loop Syndrome
Blind Loop Syndrome 		disease Digestive System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome 6 3 0.010 None 1.000 1 2017 2017
CUI: C0006288
Disease: Bronchopulmonary Sequestration
Bronchopulmonary Sequestration 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases Congenital Abnormality 6 0.010 None 1.000 1 2007 2007
CUI: C0022810
Disease: Kyasanur Forest Disease
Kyasanur Forest Disease 		disease Infections Disease or Syndrome 6 0.010 None 1.000 1 2018 2018
CUI: C0235270
Disease: Keratopathy
Keratopathy 		disease Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Disease or Syndrome 6 1 0.010 None 1.000 1 2005 2005
CUI: C0748052
Disease: Erythrodermic psoriasis
Erythrodermic psoriasis 		disease Skin and Connective Tissue Diseases Disease or Syndrome 6 0.010 None 1.000 1 2018 2018
CUI: C3854437
Disease: Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids
Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids 		disease Infections; Immune System Diseases; Nervous System Diseases Disease or Syndrome 6 0.010 None 1.000 1 2018 2018
CUI: C0264544
Disease: Adhesion of lung
Adhesion of lung 		disease Respiratory Tract Diseases Disease or Syndrome 7 0.020 None 1.000 2 1996 2001
CUI: C0011620
Disease: Stasis dermatitis
Stasis dermatitis 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Cardiovascular Diseases Disease or Syndrome 7 0.010 None 1.000 1 1999 1999
CUI: C0276430
Disease: Enterovirus meningitis
Enterovirus meningitis 		disease Infections; Nervous System Diseases Disease or Syndrome 7 0.010 None 1.000 1 2010 2010
CUI: C0334096
Disease: Intimal proliferation
Intimal proliferation 		phenotype Pathologic Function 7 0.200 None 1.000 1 1997 1997
CUI: C1735378
Disease: Chronic polyarthritis
Chronic polyarthritis 		disease Disease or Syndrome 7 0.010 None 1.000 1 1994 1994
CUI: C0155223
Disease: Dacryoadenitis
Dacryoadenitis 		disease Eye Diseases Disease or Syndrome 8 0.010 None 1.000 1 2019 2019
CUI: C3875265
Disease: Febrile urinary tract infection
Febrile urinary tract infection 		disease Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases Disease or Syndrome 8 2 0.010 None 1.000 1 2018 2018
CUI: C0268243
Disease: Niemann-Pick Disease, Type B
Niemann-Pick Disease, Type B 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 9 57 0.010 None 1.000 1 2017 2017