ITGAL, integrin subunit alpha L, 3683

N. diseases: 169; N. variants: 8
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: C3854222
Disease: Human immunodeficiency virus (HIV) II infection category B1
Human immunodeficiency virus (HIV) II infection category B1 		disease Disease or Syndrome 985 56 0.030 None 1.000 3 2003 2007
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		phenotype Laboratory Procedure 681 1322 0.100 None 1.000 2 1 2016 2019
CUI: C0272187
Disease: Congenital leukocyte adherence deficiency
Congenital leukocyte adherence deficiency 		disease Disease or Syndrome 14 12 0.020 None 1.000 2 1993 2011
CUI: C4048329
Disease: Immunosuppression
Immunosuppression 		disease Disease or Syndrome 632 9 0.020 None 1.000 2 2017 2018
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		disease Neoplastic Process 3669 502 0.020 None 1.000 2 1 2017 2019
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		phenotype Laboratory Procedure 717 1599 0.100 None 1.000 1 1 2019 2019
CUI: C0344462
Disease: Chronic lymphoproliferative disease NOS
Chronic lymphoproliferative disease NOS 		disease Neoplastic Process 3 0.010 None 1.000 1 1998 1998
CUI: C0497299
Disease: meningitis/encephalitis
meningitis/encephalitis 		disease Disease or Syndrome 5 0.010 None 1.000 1 2001 2001
CUI: C1141926
Disease: Abdominal sepsis
Abdominal sepsis 		disease Disease or Syndrome 18 0.010 None 1.000 1 2017 2017
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		phenotype Neoplastic Process 6626 169 0.010 None 1.000 1 2012 2012
CUI: C1608389
Disease: Autoimmune myocarditis
Autoimmune myocarditis 		disease Disease or Syndrome 63 0.010 None 1.000 1 2019 2019
CUI: C1735902
Disease: Acute agranulocytosis
Acute agranulocytosis 		disease Disease or Syndrome 4 0.010 None 1.000 1 1994 1994
CUI: C1744558
Disease: T-lymphocyte deficiency
T-lymphocyte deficiency 		disease Disease or Syndrome 25 0.010 None 1.000 1 1985 1985
CUI: C1868683
Disease: B-CELL MALIGNANCY, LOW-GRADE
B-CELL MALIGNANCY, LOW-GRADE 		disease Neoplastic Process 350 19 0.010 None 1.000 1 2017 2017
CUI: C2945695
Disease: Limb ischemia
Limb ischemia 		disease Disease or Syndrome 171 3 0.010 None 1.000 1 2017 2017
CUI: C4087338
Disease: Mite allergy
Mite allergy 		disease Disease or Syndrome 3 1 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: C0344315
Disease: Depressed mood
Depressed mood 		phenotype Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 1461 269 0.010 None 1.000 1 2015 2015
CUI: C0027059
Disease: Myocarditis
Myocarditis 		disease Cardiovascular Diseases Disease or Syndrome 285 2 0.020 None 1.000 2 2014 2019
CUI: C1306557
Disease: Chronic venous insufficiency
Chronic venous insufficiency 		disease Cardiovascular Diseases Disease or Syndrome 25 3 0.020 None 1.000 2 1996 1999
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		disease Cardiovascular Diseases Disease or Syndrome 2006 267 0.010 None 1.000 1 2019 2019
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		disease Cardiovascular Diseases Disease or Syndrome 2044 281 0.010 None 1.000 1 2019 2019
CUI: C0242231
Disease: Coronary Stenosis
Coronary Stenosis 		disease Cardiovascular Diseases Disease or Syndrome 111 20 0.010 None 1.000 1 2004 2004
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: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease 		group Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 757 47 0.010 None 1.000 1 1998 1998