TGM2, transglutaminase 2, 7052

N. diseases: 315; N. variants: 14
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: C0270910
Disease: Idiopathic peripheral neuropathy
Idiopathic peripheral neuropathy 		disease Nervous System Diseases Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C4525536
Disease: Hamster Fibrosarcoma
Hamster Fibrosarcoma 		disease Neoplastic Process 1 0.010 None 1.000 1 1994 1994
CUI: C0238049
Disease: Adult form of celiac disease
Adult form of celiac disease 		disease Digestive System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome 3 0.010 None 1.000 1 2000 2000
CUI: C1299614
Disease: Non-insulin-dependent diabetes mellitus with unspecified complications
Non-insulin-dependent diabetes mellitus with unspecified complications 		disease Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 4 0.200 None 1.000 3 2002 2003
CUI: C0013298
Disease: Duodenitis
Duodenitis 		disease Digestive System Diseases Disease or Syndrome 5 0.010 None 1.000 1 2009 2009
CUI: C0268118
Disease: Xanthinuria, Type I
Xanthinuria, Type I 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 5 4 0.010 None < 0.001 1 2001 2001
CUI: C3826604
Disease: Celiac disease in children
Celiac disease in children 		disease Disease or Syndrome 6 0.030 None 1.000 3 2017 2019
CUI: C0341698
Disease: Atrophy of kidney
Atrophy of kidney 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 6 1 0.010 None 1.000 1 2019 2019
CUI: C1832232
Disease: Peroxisome Biogenesis Disorder, Complementation Group C
Peroxisome Biogenesis Disorder, Complementation Group C 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 8 2 0.030 None 0.667 3 1999 2005
CUI: C0019343
Disease: Pemphigoid Gestationis
Pemphigoid Gestationis 		phenotype Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases Disease or Syndrome 8 0.010 None 1.000 1 2018 2018
CUI: C0850024
Disease: Gluten sensitivity
Gluten sensitivity 		disease Digestive System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome 11 0.030 None 1.000 3 2008 2017
CUI: C1619692
Disease: Nephrogenic Fibrosing Dermopathy
Nephrogenic Fibrosing Dermopathy 		disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 13 0.010 None 1.000 1 2007 2007
CUI: C4025285
Disease: Microspherocytosis
Microspherocytosis 		disease Disease or Syndrome 13 1 0.010 None 1.000 1 1995 1995
CUI: C0085663
Disease: Plasmacytosis
Plasmacytosis 		disease Pathological Conditions, Signs and Symptoms; Neoplasms Disease or Syndrome 15 0.010 None 1.000 1 2011 2011
CUI: C4317045
Disease: Gluten intolerance
Gluten intolerance 		disease Disease or Syndrome 16 1 0.030 None 1.000 3 2008 2017
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom 		phenotype Sign or Symptom 17 3 0.010 None 1.000 1 2017 2017
CUI: C1291314
Disease: Deficiency of monooxygenase
Deficiency of monooxygenase 		disease Disease or Syndrome 17 15 0.010 None 1.000 1 2010 2010
CUI: C0221155
Disease: Systolic hypertension
Systolic hypertension 		disease Cardiovascular Diseases Disease or Syndrome 19 1 0.010 None 1.000 1 2019 2019
CUI: C0271568
Disease: Laron Syndrome
Laron Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases Disease or Syndrome 20 26 0.010 None 1.000 1 1 2007 2007
CUI: C0028841
Disease: Ocular Hypotension
Ocular Hypotension 		disease Eye Diseases Disease or Syndrome 22 1 0.010 None 1.000 1 2018 2018
CUI: C0936016
Disease: Testicular Feminization
Testicular Feminization 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 24 7 0.010 None 1.000 1 2010 2010
CUI: C0036329
Disease: Schistosomiasis japonica
Schistosomiasis japonica 		disease Infections Disease or Syndrome 27 1 0.010 None 1.000 1 2019 2019
CUI: C0860564
Disease: Retinoic acid syndrome
Retinoic acid syndrome 		disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 29 3 0.020 None 1.000 2 2010 2019
CUI: C0342541
Disease: Precocious pubarche
Precocious pubarche 		disease Endocrine System Diseases Disease or Syndrome 30 11 0.010 None 1.000 1 1 2002 2002
CUI: C2718067
Disease: Alcoholic Steatohepatitis
Alcoholic Steatohepatitis 		disease Digestive System Diseases; Chemically-Induced Disorders Disease or Syndrome 30 0.010 None 1.000 1 2009 2009