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: C0019348
Disease: Herpes Simplex Infections
Herpes Simplex Infections
group Infections; Skin and Connective Tissue Diseases Disease or Syndrome 645 11 0.010 None < 0.001 1 1986 1986
CUI: C1282609
Disease: Granulocytosis
Granulocytosis
disease Hemic and Lymphatic Diseases Disease or Syndrome 15 1 0.010 None 1.000 1 1987 1987
CUI: C0021051
Disease: Immunologic Deficiency Syndromes
Immunologic Deficiency Syndromes
group Immune System Diseases Disease or Syndrome 973 31 0.010 None 1.000 1 1990 1990
CUI: C0334663
Disease: Histiocytic sarcoma
Histiocytic sarcoma
disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 69 8 0.010 None 1.000 1 1991 1991
CUI: C0026948
Disease: Mycosis Fungoides
Mycosis Fungoides
group Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 251 8 0.010 None 1.000 1 1991 1991
CUI: C0024419
Disease: Waldenstrom Macroglobulinemia
Waldenstrom Macroglobulinemia
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Neoplastic Process 162 15 0.010 None 1.000 1 1991 1991
CUI: C0276447
Disease: Rhinovirus infection
Rhinovirus infection
disease Infections Disease or Syndrome 202 4 0.010 None 1.000 1 1992 1992
CUI: C0026499
Disease: Monosomy
Monosomy
group Pathological Conditions, Signs and Symptoms Congenital Abnormality 214 11 0.010 None 1.000 1 1992 1992
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 1447 291 0.010 None 1.000 1 1993 1993
CUI: C0949691
Disease: Spondylarthropathies
Spondylarthropathies
group Musculoskeletal Diseases Disease or Syndrome 92 7 0.010 None 1.000 1 1993 1993
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 1293 222 0.010 None 1.000 1 1993 1993
Respiratory Distress Syndrome, Adult
disease Respiratory Tract Diseases Disease or Syndrome 434 60 0.010 None 1.000 1 1994 1994
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: C0031106
Disease: Aggressive Periodontitis
Aggressive Periodontitis
disease Stomatognathic Diseases Disease or Syndrome 184 59 0.020 None 1.000 2 1987 1995
CUI: C0023448
Disease: Lymphoid leukemia
Lymphoid leukemia
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 288 4 0.010 None 1.000 1 1995 1995
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
disease Digestive System Diseases Disease or Syndrome 1458 827 0.010 None 1.000 1 1995 1995
CUI: C0017574
Disease: Gingivitis
Gingivitis
disease Infections; Stomatognathic Diseases Disease or Syndrome 152 3 0.010 None 1.000 1 1995 1995
CUI: C0028259
Disease: Nodule
Nodule
phenotype Acquired Abnormality 278 19 0.010 None 1.000 1 1996 1996
CUI: C0023479
Disease: Acute myelomonocytic leukemia
Acute myelomonocytic leukemia
disease Neoplasms Neoplastic Process 105 3 0.010 None 1.000 1 1997 1997
CUI: C0031094
Disease: Periodontal Pocket
Periodontal Pocket
disease Stomatognathic Diseases Anatomical Abnormality 28 0.010 None 1.000 1 1997 1997
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
Human immunodeficiency virus (HIV) II infection category B1
disease Disease or Syndrome 985 56 0.010 None 1.000 1 1998 1998
CUI: C0018213
Disease: Graves Disease
Graves Disease
disease Eye Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome 585 352 0.010 None 1.000 1 1998 1998
CUI: C0015397
Disease: Disorder of eye
Disorder of eye
group Eye Diseases Disease or Syndrome 400 14 0.010 None < 0.001 1 1998 1998
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