TRIM21, tripartite motif containing 21, 6737

N. diseases: 229; N. variants: 1
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: C0267663
Disease: Congenital secretory diarrhea, sodium type (disorder)
Congenital secretory diarrhea, sodium type (disorder) 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Congenital Abnormality 18 17 0.010 None 1.000 1 2017 2017
CUI: C0149530
Disease: Congenital heart block
Congenital heart block 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome; Congenital Abnormality 20 2 0.100 None 1.000 25 1989 2019
CUI: C0151450
Disease: Secondary Sjögren's syndrome
Secondary Sjögren's syndrome 		disease Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases Disease or Syndrome 20 0.010 None 1.000 1 1996 1996
CUI: C0334307
Disease: Tubulovillous adenoma
Tubulovillous adenoma 		disease Neoplasms Neoplastic Process 20 0.010 None 1.000 1 2012 2012
CUI: C0850639
Disease: premalignant lesion
premalignant lesion 		phenotype Neoplastic Process 20 5 0.010 None 1.000 1 2018 2018
CUI: C0268380
Disease: Systemic amyloidosis
Systemic amyloidosis 		disease Nutritional and Metabolic Diseases Disease or Syndrome 21 10 0.010 None 1.000 1 2010 2010
CUI: C0409979
Disease: Neonatal Systemic lupus erythematosus
Neonatal Systemic lupus erythematosus 		disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 22 1 0.100 None 1.000 23 1984 2017
CUI: C0264545
Disease: Thickening of pleura
Thickening of pleura 		disease Respiratory Tract Diseases Disease or Syndrome 25 0.010 None 1.000 1 2020 2020
CUI: C0281479
Disease: Primary Systemic Amyloidosis
Primary Systemic Amyloidosis 		disease Neoplasms; Nutritional and Metabolic Diseases; Immune System Diseases Neoplastic Process 27 10 0.010 None 1.000 1 2010 2010
CUI: C0919659
Disease: Oropharyngeal candidiasis
Oropharyngeal candidiasis 		disease Infections Disease or Syndrome 27 3 0.010 None 1.000 1 2017 2017
CUI: C0085624
Disease: Burning sensation
Burning sensation 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 30 0.010 None 1.000 1 2017 2017
CUI: C0023643
Disease: Lichen disease
Lichen disease 		disease Skin and Connective Tissue Diseases Disease or Syndrome 33 0.010 None 1.000 1 2018 2018
CUI: C0729531
Disease: Viral respiratory infection
Viral respiratory infection 		group Infections; Respiratory Tract Diseases Disease or Syndrome 33 0.010 None 1.000 1 2017 2017
CUI: C3276706
Disease: Small Fiber Neuropathy
Small Fiber Neuropathy 		disease Nervous System Diseases Disease or Syndrome 35 8 0.010 None 1.000 1 2019 2019
CUI: C0020455
Disease: Hypergammaglobulinemia
Hypergammaglobulinemia 		disease Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 36 0.020 None 1.000 2 2018 2019
CUI: C0007930
Disease: Chagas Cardiomyopathy
Chagas Cardiomyopathy 		disease Infections; Cardiovascular Diseases Disease or Syndrome 37 8 0.010 None 1.000 1 2011 2011
CUI: C2895206
Disease: Autoimmune disease (systemic) NOS
Autoimmune disease (systemic) NOS 		disease Disease or Syndrome 37 3 0.010 None 1.000 1 2009 2009
CUI: C0024140
Disease: Lupus Erythematosus, Subacute Cutaneous
Lupus Erythematosus, Subacute Cutaneous 		disease Skin and Connective Tissue Diseases Disease or Syndrome 39 1 0.030 None 1.000 3 1991 2008
CUI: C0024137
Disease: Lupus Erythematosus, Cutaneous
Lupus Erythematosus, Cutaneous 		disease Skin and Connective Tissue Diseases Disease or Syndrome 39 7 0.020 None 1.000 2 2009 2017
CUI: C0265797
Disease: Congenital emphysema
Congenital emphysema 		disease Respiratory Tract Diseases Congenital Abnormality 40 0.020 None 1.000 2 2009 2017
CUI: C0035854
Disease: Rosacea
Rosacea 		disease Skin and Connective Tissue Diseases Disease or Syndrome 41 2 0.010 None 1.000 1 2018 2018
CUI: C0264886
Disease: Conduction disorder of the heart
Conduction disorder of the heart 		group Cardiovascular Diseases Disease or Syndrome 41 11 0.010 None 1.000 1 1992 1992
CUI: C0037023
Disease: Sialadenitis
Sialadenitis 		disease Stomatognathic Diseases Disease or Syndrome 42 0.010 None 1.000 1 2019 2019
CUI: C0272242
Disease: Complement deficiency disease
Complement deficiency disease 		group Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 42 0.010 None 1.000 1 1988 1988
CUI: C0393639
Disease: Hashimoto's encephalitis
Hashimoto's encephalitis 		disease Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 47 0.010 None < 0.001 1 2018 2018