LMAN1, lectin, mannose binding 1, 3998

N. diseases: 30; N. variants: 6
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.
Familial Multiple Coagulation Factor Deficiency I
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 2 6 0.700 definitive 1.000 9 5 1998 2011
FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 7 0.400 None 1.000 15 1998 2019
CUI: C0883409
Disease: Cardiac troponin I measurement
Cardiac troponin I measurement
phenotype Laboratory Procedure 11 14 0.100 None 1.000 1 1 2019 2019
CUI: C4317320
Disease: Factor V deficiency
Factor V deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 6 1 0.100 None 0
CUI: C4025649
Disease: Reduced factor VIII activity
Reduced factor VIII activity
phenotype Finding 4 1 0.100 None 0
CUI: C1458140
Disease: Bleeding tendency
Bleeding tendency
phenotype Hemic and Lymphatic Diseases Pathologic Function 71 14 0.100 None 0
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group Hemic and Lymphatic Diseases Disease or Syndrome 267 31 0.080 None 1.000 8 1999 2013
Familial multiple factor deficiency syndrome, type I
disease Disease or Syndrome 4 0.040 None 1.000 4 2004 2011
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 143 295 0.030 None 1.000 3 1999 2008
CUI: C3494187
Disease: Factor VIII Deficiency
Factor VIII Deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 9 1 0.030 None 1.000 3 1999 2008
Coagulation factor deficiency syndrome
group Hemic and Lymphatic Diseases Disease or Syndrome 13 2 0.020 None 1.000 2 2004 2012
CUI: C3714514
Disease: Infection
Infection
group Infections Pathologic Function 491 0.020 None 1.000 2 2005 2007
CUI: C2873785
Disease: Deficiency of factor V [labile]
Deficiency of factor V [labile]
disease Disease or Syndrome 3 0.020 None 0.500 2 2005 2011
VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 6 4 0.010 None 1.000 1 2004 2004
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
disease Cardiovascular Diseases Disease or Syndrome 1708 1577 0.010 None 1.000 1 2013 2013
Microsatellite instability-high colorectal cancer
disease Digestive System Diseases; Neoplasms Neoplastic Process 26 4 0.010 None 1.000 1 2009 2009
Congenital dyserythropoietic anemia, type II
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 21 14 0.010 None 1.000 1 2012 2012
CUI: C1300257
Disease: Thanatophoric dysplasia, type 2
Thanatophoric dysplasia, type 2
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 11 17 0.010 None 1.000 1 2008 2008
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
phenotype Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 6243 355 0.010 None 1.000 1 2009 2009
CUI: C0007097
Disease: Carcinoma
Carcinoma
group Neoplasms Neoplastic Process 2462 103 0.010 None 1.000 1 2009 2009
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
group Digestive System Diseases; Neoplasms Neoplastic Process 1296 609 0.010 None 1.000 1 2009 2009
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
disease Cardiovascular Diseases Disease or Syndrome 1282 440 0.010 None 1.000 1 2013 2013
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
disease Cardiovascular Diseases Disease or Syndrome 1576 1178 0.010 None 1.000 1 2013 2013
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases Disease or Syndrome 456 130 0.010 None 1.000 1 1997 1997
CUI: C0018939
Disease: Hematological Disease
Hematological Disease
group Hemic and Lymphatic Diseases Disease or Syndrome 255 16 0.010 None 1.000 1 2012 2012