ITGAM, integrin subunit alpha M, 3684

N. diseases: 343; N. variants: 14
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: C0752334
Disease: Lupus Meningoencephalitis
Lupus Meningoencephalitis 		disease Infections; Skin and Connective Tissue Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 3 0.300 None 1.000 1 2016 2016
CUI: C1735902
Disease: Acute agranulocytosis
Acute agranulocytosis 		disease Disease or Syndrome 4 0.020 None 1.000 2 1994 2002
CUI: C1845609
Disease: Lymphoid depletion
Lymphoid depletion 		disease Disease or Syndrome 4 0.010 None 1.000 1 2001 2001
CUI: C0497299
Disease: meningitis/encephalitis
meningitis/encephalitis 		disease Disease or Syndrome 5 0.010 None 1.000 1 2001 2001
CUI: C2717750
Disease: Platelet alpha-Granule Deficiency
Platelet alpha-Granule Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 5 0.010 None 1.000 1 2018 2018
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 1999 1999
CUI: C0752332
Disease: Lupus Vasculitis, Central Nervous System
Lupus Vasculitis, Central Nervous System 		disease Infections; Skin and Connective Tissue Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 7 0.300 None 1.000 1 2016 2016
CUI: C4329780
Disease: Early T Acute Lymphoblastic Leukemia
Early T Acute Lymphoblastic Leukemia 		disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 7 0.010 None 1.000 1 2019 2019
CUI: C0240903
Disease: Rheumatoid Vasculitis
Rheumatoid Vasculitis 		disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Cardiovascular Diseases Disease or Syndrome 9 0.010 None 1.000 1 2001 2001
CUI: C4285778
Disease: Systemic bacterial infection
Systemic bacterial infection 		disease Disease or Syndrome 9 0.010 None 1.000 1 2001 2001
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: C3536663
Disease: Acute deep venous thrombosis
Acute deep venous thrombosis 		disease Cardiovascular Diseases Disease or Syndrome 11 0.010 None 1.000 1 2005 2005
CUI: C0272187
Disease: Congenital leukocyte adherence deficiency
Congenital leukocyte adherence deficiency 		disease Disease or Syndrome 14 12 0.080 None 1.000 8 1990 2011
CUI: C1282609
Disease: Granulocytosis
Granulocytosis 		disease Hemic and Lymphatic Diseases Disease or Syndrome 15 1 0.010 None 1.000 1 1987 1987
CUI: C0151950
Disease: Deep thrombophlebitis
Deep thrombophlebitis 		disease Cardiovascular Diseases Disease or Syndrome 16 0.010 None < 0.001 1 2005 2005
CUI: C4022459
Disease: Decreased adipose tissue
Decreased adipose tissue 		phenotype Sign or Symptom 17 0.020 None 1.000 2 2019 2019
CUI: C1141926
Disease: Abdominal sepsis
Abdominal sepsis 		disease Disease or Syndrome 18 0.010 None 1.000 1 2017 2017
CUI: C4551910
Disease: Acute Inflammatory Demyelinating Polyneuropathy
Acute Inflammatory Demyelinating Polyneuropathy 		disease Immune System Diseases; Nervous System Diseases Disease or Syndrome 19 2 0.010 None 1.000 1 2016 2016
CUI: C0399447
Disease: Early onset periodontitis
Early onset periodontitis 		disease Stomatognathic Diseases Disease or Syndrome 21 0.020 None 1.000 2 1987 1995
CUI: C1142339
Disease: Intestinal adenoma
Intestinal adenoma 		disease Neoplastic Process 23 0.010 None 1.000 1 2015 2015
CUI: C0036974
Disease: Shock
Shock 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 25 0.010 None 1.000 1 2006 2006
CUI: C0086647
Disease: Mucopolysaccharidosis Type IIIA
Mucopolysaccharidosis Type IIIA 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 25 69 0.010 None 1.000 1 2013 2013
CUI: C0235820
Disease: Neonatal encephalopathy
Neonatal encephalopathy 		disease Nervous System Diseases Disease or Syndrome 26 10 0.010 None 1.000 1 2015 2015
CUI: C1257963
Disease: Endogenous Hyperinsulinism
Endogenous Hyperinsulinism 		disease Nutritional and Metabolic Diseases Disease or Syndrome 26 0.300 None 1.000 1 2018 2018
CUI: C1257964
Disease: Exogenous Hyperinsulinism
Exogenous Hyperinsulinism 		disease Nutritional and Metabolic Diseases Disease or Syndrome 26 0.300 None 1.000 1 2018 2018