CD14, CD14 molecule, 929

N. diseases: 551; 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.
Mucosa-Associated Lymphoid Tissue Lymphoma
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 264 13 0.010 None 1.000 1 2009 2009
Childhood Diffuse Large Cell Lymphoma
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 39 0.010 None 1.000 1 2014 2014
CUI: C0278878
Disease: Adult Glioblastoma
Adult Glioblastoma
disease Neoplasms Neoplastic Process 2528 98 0.010 None 1.000 1 2010 2010
Liver and Intrahepatic Biliary Tract Carcinoma
disease Digestive System Diseases; Neoplasms Neoplastic Process 1395 73 0.010 None 1.000 1 2019 2019
Squamous cell carcinoma of esophagus
disease Digestive System Diseases; Neoplasms Neoplastic Process 2053 329 0.010 None 1.000 1 2014 2014
Conventional (Clear Cell) Renal Cell Carcinoma
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Neoplastic Process 2346 222 0.010 None 1.000 1 2011 2011
CUI: C0280217
Disease: stage, non-small cell lung cancer
stage, non-small cell lung cancer
disease Neoplasms; Respiratory Tract Diseases Neoplastic Process 107 6 0.010 None 1.000 1 2010 2010
CUI: C0280449
Disease: secondary acute myeloid leukemia
secondary acute myeloid leukemia
disease Neoplasms Neoplastic Process 91 8 0.010 None 1.000 1 2001 2001
CUI: C0280474
Disease: Childhood Glioblastoma
Childhood Glioblastoma
disease Neoplasms Neoplastic Process 2527 98 0.010 None 1.000 1 2010 2010
CUI: C0282160
Disease: Aplasia Cutis Congenita
Aplasia Cutis Congenita
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Congenital Abnormality 393 14 0.010 None 1.000 1 2010 2010
CUI: C0302362
Disease: Brucella melitensis infection
Brucella melitensis infection
disease Infections Disease or Syndrome 17 0.010 None 1.000 1 2017 2017
CUI: C0302486
Disease: Erythrophagocytosis
Erythrophagocytosis
disease Disease or Syndrome 40 0.010 None 1.000 1 2016 2016
CUI: C0278762
Disease: Adult Diffuse Large Cell Lymphoma
Adult Diffuse Large Cell Lymphoma
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 39 0.010 None 1.000 1 2014 2014
CUI: C0277528
Disease: Traveler's diarrhea
Traveler's diarrhea
disease Digestive System Diseases; Infections Disease or Syndrome 21 2 0.010 None 1.000 1 1 2011 2011
CUI: C0276668
Disease: Coccidioidal granuloma
Coccidioidal granuloma
phenotype Pathological Conditions, Signs and Symptoms; Infections; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C0242723
Disease: Parasitemia
Parasitemia
disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 140 3 0.010 None 1.000 1 2017 2017
CUI: C0262655
Disease: Recurrent urinary tract infection
Recurrent urinary tract infection
disease Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases Disease or Syndrome 237 21 0.010 None 1.000 1 2011 2011
CUI: C0263678
Disease: Acute arthritis
Acute arthritis
disease Musculoskeletal Diseases Disease or Syndrome 9 0.010 None 1.000 1 2002 2002
CUI: C0264413
Disease: Late onset asthma
Late onset asthma
disease Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 9 0.010 None 1.000 1 2017 2017
CUI: C0264423
Disease: Asthma, Occupational
Asthma, Occupational
disease Respiratory Tract Diseases; Immune System Diseases; Occupational Diseases Disease or Syndrome 42 2 0.010 None 1.000 1 2016 2016
CUI: C0264684
Disease: Coronary arteritis
Coronary arteritis
disease Cardiovascular Diseases Disease or Syndrome 6 0.010 None 1.000 1 2012 2012
CUI: C0264716
Disease: Chronic heart failure
Chronic heart failure
disease Cardiovascular Diseases Disease or Syndrome 223 11 0.010 None 1.000 1 2006 2006
CUI: C0265219
Disease: Miller Dieker syndrome
Miller Dieker syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 182 9 0.010 None 1.000 1 2014 2014
CUI: C0265338
Disease: Coffin-Siris syndrome
Coffin-Siris syndrome
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Stomatognathic Diseases; Behavior and Behavior Mechanisms Disease or Syndrome 56 6 0.010 None 1.000 1 2019 2019
Congenital glucose-galactose malabsorption
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome; Congenital Abnormality 19 12 0.010 None 1.000 1 1995 1995