S100A9, S100 calcium binding protein A9, 6280

N. diseases: 363; N. variants: 2
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: C0857035
Disease: Acute anaphylaxis
Acute anaphylaxis 		disease Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C1266100
Disease: Carcinoma showing thymus-like element
Carcinoma showing thymus-like element 		disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 2 0.010 None 1.000 1 2006 2006
CUI: C0751004
Disease: Giant Intracranial Aneurysm
Giant Intracranial Aneurysm 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 3 0.010 None 1.000 1 2019 2019
CUI: C1860229
Disease: Hyperzincemia and Hypercalprotectinemia
Hyperzincemia and Hypercalprotectinemia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 3 0.010 None 1.000 1 2015 2015
CUI: C0155883
Disease: Chronic obstructive asthma (with obstructive pulmonary disease)
Chronic obstructive asthma (with obstructive pulmonary disease) 		disease Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 4 1 0.010 None 1.000 1 2015 2015
CUI: C0264480
Disease: Bakers' asthma
Bakers' asthma 		disease Pathological Conditions, Signs and Symptoms; Infections; Respiratory Tract Diseases; Immune System Diseases; Occupational Diseases Disease or Syndrome 5 0.010 None 1.000 1 2015 2015
CUI: C0006261
Disease: Bronchial Diseases
Bronchial Diseases 		group Respiratory Tract Diseases Disease or Syndrome 6 0.010 None 1.000 1 2003 2003
CUI: C1862324
Disease: Elliptocytosis 4
Elliptocytosis 4 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 6 0.010 None 1.000 1 2012 2012
CUI: C0745581
Disease: knee symptoms
knee symptoms 		phenotype Sign or Symptom 7 0.010 None 1.000 1 2019 2019
CUI: C0853954
Disease: Corneal calcification
Corneal calcification 		phenotype Anatomical Abnormality 10 0.010 None 1.000 1 2017 2017
CUI: C0015929
Disease: Fetal Diseases
Fetal Diseases 		group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 11 0.010 None 1.000 1 2003 2003
CUI: C1708371
Disease: Histiocytoid Cardiomyopathy
Histiocytoid Cardiomyopathy 		disease Cardiovascular Diseases Disease or Syndrome 12 3 0.010 None 1.000 1 2012 2012
CUI: C4075512
Disease: Flap necrosis
Flap necrosis 		disease Disease or Syndrome 12 0.010 None 1.000 1 2017 2017
CUI: C0240803
Disease: Primary cerebral lymphoma
Primary cerebral lymphoma 		disease Neoplasms; Immune System Diseases; Nervous System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 13 0.010 None 1.000 1 2005 2005
CUI: C2678439
Disease: CRANIOOSTEOARTHROPATHY
CRANIOOSTEOARTHROPATHY 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 13 1 0.010 None 1.000 1 2015 2015
CUI: C0684550
Disease: Secondary malignant neoplasm of vertebral column
Secondary malignant neoplasm of vertebral column 		disease Neoplastic Process 15 0.010 None 1.000 1 2018 2018
CUI: C0085694
Disease: Chronic cholecystitis
Chronic cholecystitis 		disease Digestive System Diseases Disease or Syndrome 16 0.010 None 1.000 1 2013 2013
CUI: C1141926
Disease: Abdominal sepsis
Abdominal sepsis 		disease Disease or Syndrome 18 0.020 None 1.000 2 2007 2009
CUI: C4068858
Disease: Avascular retina
Avascular retina 		disease Disease or Syndrome 19 0.010 None 1.000 1 2011 2011
CUI: C0332447
Disease: Morphologically abnormal structure (morphologic abnormality)
Morphologically abnormal structure (morphologic abnormality) 		group Anatomical Abnormality 20 0.010 None 1.000 1 2005 2005
CUI: C0919909
Disease: Tonic clonic movements
Tonic clonic movements 		disease Disease or Syndrome 22 0.010 None 1.000 1 2016 2016
CUI: C0018188
Disease: Granuloma
Granuloma 		phenotype Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases Pathologic Function 24 0.010 None 1.000 1 2007 2007
CUI: C0011389
Disease: Dental Plaque
Dental Plaque 		phenotype Stomatognathic Diseases Disease or Syndrome 27 0.010 None 1.000 1 2011 2011
CUI: C0079293
Disease: Epidermolysis Bullosa Acquisita
Epidermolysis Bullosa Acquisita 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 32 0.010 None 1.000 1 2016 2016
CUI: C2931133
Disease: Pediatric Crohn's disease
Pediatric Crohn's disease 		disease Digestive System Diseases Disease or Syndrome 32 6 0.010 None 1.000 1 2014 2014