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.
Congenital hypoplasia of adrenal gland
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases Congenital Abnormality 45 13 0.010 None 1.000 1 2018 2018
CUI: C0262655
Disease: Recurrent urinary tract infection
Recurrent urinary tract infection
disease Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases Disease or Syndrome 237 21 0.010 None 1.000 1 2006 2006
CUI: C0262988
Disease: Vasculitis of the skin
Vasculitis of the skin
disease Skin and Connective Tissue Diseases; Cardiovascular Diseases Disease or Syndrome 21 1 0.010 None 1.000 1 2013 2013
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: C0264757
Disease: Rheumatic disease of heart valve
Rheumatic disease of heart valve
disease Infections; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases Disease or Syndrome 11 0.010 None 1.000 1 2017 2017
CUI: C0265223
Disease: Cohen syndrome
Cohen syndrome
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Congenital Abnormality 10 292 0.010 None 1.000 1 2019 2019
CUI: C0265706
Disease: Gastroschisis
Gastroschisis
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 31 8 0.010 None 1.000 1 1 2006 2006
CUI: C0265962
Disease: Ichthyosis linearis circumflexa
Ichthyosis linearis circumflexa
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome; Congenital Abnormality 64 20 0.010 None 1.000 1 2000 2000
CUI: C0267750
Disease: Acute peritonitis
Acute peritonitis
disease Digestive System Diseases; Infections Disease or Syndrome 10 0.010 None 1.000 1 2014 2014
CUI: C0268095
Disease: Keshan disease
Keshan disease
disease Infections; Cardiovascular Diseases Disease or Syndrome 17 1 0.010 None 1.000 1 2014 2014
Xeroderma Pigmentosum, Complementation Group D
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 70 111 0.010 None 1.000 1 1997 1997
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
CUI: C0268398
Disease: Familial lichen amyloidosis
Familial lichen amyloidosis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 230 24 0.010 None 1.000 1 1999 1999
CUI: C0275518
Disease: Acute infectious disease
Acute infectious disease
group Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 198 5 0.010 None 1.000 1 2017 2017
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: C0278488
Disease: Carcinoma breast stage IV
Carcinoma breast stage IV
disease Neoplastic Process 573 14 0.010 None < 0.001 1 2017 2017
Systemic Inflammatory Response Syndrome
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 185 9 0.010 None 1.000 1 2018 2018
CUI: C0242723
Disease: Parasitemia
Parasitemia
disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 140 3 0.010 None 1.000 1 2011 2011
Rapidly progressive glomerulonephritis
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 19 1 0.010 None 1.000 1 2008 2008
CUI: C0221505
Disease: Lesion of brain
Lesion of brain
group Disease or Syndrome 188 9 0.010 None 1.000 1 2017 2017
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
phenotype Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 910 121 0.010 None 1.000 1 2019 2019
CUI: C0234985
Disease: Mental deterioration
Mental deterioration
phenotype Mental Disorders Mental or Behavioral Dysfunction 508 121 0.010 None 1.000 1 2003 2003
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: C0235272
Disease: Retinal damage
Retinal damage
phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases; Wounds and Injuries Disease or Syndrome 32 1 0.010 None 1.000 1 2017 2017
CUI: C0235522
Disease: Disorder of vein
Disorder of vein
group Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 16 1 0.010 None 1.000 1 1999 1999