CCL21, C-C motif chemokine ligand 21, 6366

N. diseases: 179; N. variants: 3
Source: BEFREE ×
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: C1719796
Disease: With-the-rule astigmatism
With-the-rule astigmatism 		disease Eye Diseases Disease or Syndrome 1 0.010 None 1.000 1 2019 2019
CUI: C0729842
Disease: Serpiginous choroiditis
Serpiginous choroiditis 		disease Eye Diseases Disease or Syndrome 3 0.010 None 1.000 1 2018 2018
CUI: C0741183
Disease: aortic stenosis symptomatic
aortic stenosis symptomatic 		disease Disease or Syndrome 3 0.010 None 1.000 1 2014 2014
CUI: C1306878
Disease: Climacteric discomfort
Climacteric discomfort 		phenotype Sign or Symptom 4 0.010 None 1.000 1 2013 2013
CUI: C1959583
Disease: Myocardial Failure
Myocardial Failure 		disease Cardiovascular Diseases Disease or Syndrome 7 0.010 None 1.000 1 2012 2012
CUI: C0006060
Disease: Boutonneuse Fever
Boutonneuse Fever 		disease Infections Disease or Syndrome 10 3 0.010 None 1.000 1 2014 2014
CUI: C0012243
Disease: Digestive System Neoplasms
Digestive System Neoplasms 		group Digestive System Diseases; Neoplasms Neoplastic Process 10 2 0.010 None 1.000 1 2018 2018
CUI: C4743661
Disease: Leukocyte Adhesion Deficiency Type 3
Leukocyte Adhesion Deficiency Type 3 		disease Disease or Syndrome 11 3 0.010 None 1.000 1 2011 2011
CUI: C1692871
Disease: Inflammatory polyarthritis
Inflammatory polyarthritis 		disease Disease or Syndrome 13 1 0.010 None 1.000 1 2010 2010
CUI: C1863844
Disease: Adult-onset citrullinemia type 2
Adult-onset citrullinemia type 2 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 14 1 0.010 None 1.000 1 2019 2019
CUI: C3495890
Disease: Osteochondral defects
Osteochondral defects 		phenotype Anatomical Abnormality 17 0.010 None 1.000 1 2019 2019
CUI: C0010691
Disease: Cystinuria
Cystinuria 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 20 7 0.010 None 1.000 1 2019 2019
CUI: C0030293
Disease: Pancreatic Insufficiency
Pancreatic Insufficiency 		disease Digestive System Diseases Disease or Syndrome 21 23 0.010 None 1.000 1 2018 2018
CUI: C0268647
Disease: Lysinuric Protein Intolerance
Lysinuric Protein Intolerance 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 21 1 0.010 None 1.000 1 2019 2019
CUI: C0947912
Disease: Myasthenias
Myasthenias 		disease Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 21 2 0.010 None 1.000 1 2009 2009
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 24 10 0.010 None 1.000 1 1996 1996
CUI: C0040115
Disease: Thymus Hyperplasia
Thymus Hyperplasia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 26 0.010 None 1.000 1 2009 2009
CUI: C0004106
Disease: Astigmatism
Astigmatism 		disease Eye Diseases Disease or Syndrome 28 2 0.010 None 1.000 1 2019 2019
CUI: C1849718
Disease: POPLITEAL PTERYGIUM SYNDROME, LETHAL TYPE
POPLITEAL PTERYGIUM SYNDROME, LETHAL TYPE 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Musculoskeletal Diseases; Stomatognathic Diseases Disease or Syndrome 29 2 0.010 None 1.000 1 2016 2016
CUI: C0267963
Disease: Exocrine pancreatic insufficiency
Exocrine pancreatic insufficiency 		disease Digestive System Diseases Disease or Syndrome 41 23 0.010 None 1.000 1 2018 2018
CUI: C0014527
Disease: Epidermolysis Bullosa
Epidermolysis Bullosa 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Congenital Abnormality 45 3 0.010 None 1.000 1 2017 2017
CUI: C4721509
Disease: Usual Interstitial Pneumonia
Usual Interstitial Pneumonia 		disease Respiratory Tract Diseases Disease or Syndrome 49 2 0.010 None 1.000 1 2007 2007
CUI: C0007760
Disease: Cerebellar Diseases
Cerebellar Diseases 		group Nervous System Diseases Disease or Syndrome 58 4 0.010 None 1.000 1 2013 2013
CUI: C0263666
Disease: Dermatomyositis, Childhood Type
Dermatomyositis, Childhood Type 		disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 59 0.020 None 1.000 2 2007 2016
CUI: C0085435
Disease: Arthritis, Reactive
Arthritis, Reactive 		disease Infections; Musculoskeletal Diseases Disease or Syndrome 62 2 0.010 None 1.000 1 2007 2007