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.
CUI: C1273976
Disease: First myocardial infarction
First myocardial infarction 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 17 7 0.010 None 1.000 1 2007 2007
CUI: C0035457
Disease: Rhinitis, Allergic, Perennial
Rhinitis, Allergic, Perennial 		disease Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 18 0.010 None 1.000 1 2006 2006
CUI: C0162848
Disease: Lichenoid Eruptions
Lichenoid Eruptions 		group Skin and Connective Tissue Diseases Disease or Syndrome 18 0.010 None 1.000 1 2019 2019
CUI: C0019623
Disease: Malignant histiocytosis
Malignant histiocytosis 		disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 19 2 0.010 None 1.000 1 1991 1991
CUI: C0268186
Disease: Congenital glucose-galactose malabsorption
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
CUI: C0729777
Disease: Corneal Infection
Corneal Infection 		disease Infections; Eye Diseases Disease or Syndrome 20 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: C0936250
Disease: Eczema Herpeticum
Eczema Herpeticum 		disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 21 4 0.010 None 1.000 1 2014 2014
CUI: C1399793
Disease: skin fold (abnormality)
skin fold (abnormality) 		disease Anatomical Abnormality 21 8 0.010 None 1.000 1 2018 2018
CUI: C4289792
Disease: Chronic Active EBV Infection of T-and NK-Cell Type, Systemic Form
Chronic Active EBV Infection of T-and NK-Cell Type, Systemic Form 		disease Infections Disease or Syndrome 22 0.010 None 1.000 1 2017 2017
CUI: C4049273
Disease: Systemic immune activation
Systemic immune activation 		disease Disease or Syndrome 23 0.020 None 1.000 2 2002 2016
CUI: C0342881
Disease: Familial hypercholesterolemia - homozygous
Familial hypercholesterolemia - homozygous 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 23 72 0.010 None 1.000 1 1998 1998
CUI: C2825139
Disease: Acute Myeloid Leukemia with Myelodysplasia-Related Changes
Acute Myeloid Leukemia with Myelodysplasia-Related Changes 		disease Neoplasms Neoplastic Process 23 0.010 None 1.000 1 2017 2017
CUI: C3874381
Disease: Childhood nephrotic syndrome
Childhood nephrotic syndrome 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 23 6 0.010 None 1.000 1 2003 2003
CUI: C0085423
Disease: Gram-Negative Bacterial Infections
Gram-Negative Bacterial Infections 		group Infections Disease or Syndrome 24 3 0.030 None 1.000 3 2005 2009
CUI: C0271429
Disease: Acute otitis media
Acute otitis media 		disease Otorhinolaryngologic Diseases Disease or Syndrome 24 1 0.010 None 1.000 1 2006 2006
CUI: C0026766
Disease: Multiple Organ Failure
Multiple Organ Failure 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 25 0.010 None 1.000 1 1998 1998
CUI: C1719498
Disease: Generalized chronic periodontitis
Generalized chronic periodontitis 		disease Stomatognathic Diseases Disease or Syndrome 25 4 0.010 None 1.000 1 1 2017 2017
CUI: C3889136
Disease: Tumor Necrosis Factor Receptor 1-Associated Periodic Syndrome
Tumor Necrosis Factor Receptor 1-Associated Periodic Syndrome 		disease Disease or Syndrome 25 8 0.010 None 1.000 1 2007 2007
CUI: C0282667
Disease: Infant, Very Low Birth Weight
Infant, Very Low Birth Weight 		disease Disease or Syndrome 26 1 0.020 None 0.500 2 2006 2006
CUI: C0006430
Disease: Burning Mouth Syndrome
Burning Mouth Syndrome 		disease Stomatognathic Diseases Disease or Syndrome 26 1 0.010 None 1.000 1 2008 2008
CUI: C0008340
Disease: Choledochal Cyst
Choledochal Cyst 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms Congenital Abnormality 27 0.010 None 1.000 1 2010 2010
CUI: C0151814
Disease: Coronary Occlusion
Coronary Occlusion 		disease Cardiovascular Diseases Disease or Syndrome 28 1 0.010 None 1.000 1 2000 2000
CUI: C0947961
Disease: Atopic disorders
Atopic disorders 		group Disease or Syndrome 29 2 0.020 None 1.000 2 1 2004 2005
CUI: C0041330
Disease: Tuberculosis, Spinal
Tuberculosis, Spinal 		disease Infections; Musculoskeletal Diseases Disease or Syndrome 29 8 0.010 None 1.000 1 2018 2018