DPP4, dipeptidyl peptidase 4, 1803

N. diseases: 451; N. variants: 13
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: C0333243
Disease: Pitting edema
Pitting edema 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 1 0.010 None 1.000 1 2019 2019
CUI: C0948119
Disease: Ovarian fibrosis
Ovarian fibrosis 		disease Disease or Syndrome 1 0.010 None 1.000 1 2019 2019
CUI: C0263419
Disease: Reactive perforating collagenosis
Reactive perforating collagenosis 		disease Disease or Syndrome 2 0.010 None 1.000 1 2018 2018
CUI: C4520892
Disease: Otospondylomegaepiphyseal dysplasia
Otospondylomegaepiphyseal dysplasia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases Disease or Syndrome 3 5 0.010 None 1.000 1 2017 2017
CUI: C1696153
Disease: Remitting seronegative symmetrical synovitis with pitting oedema syndrome
Remitting seronegative symmetrical synovitis with pitting oedema syndrome 		disease Disease or Syndrome 4 0.010 None 1.000 1 2019 2019
CUI: C0741395
Disease: back pain mechanical
back pain mechanical 		phenotype Sign or Symptom 5 0.010 None 1.000 1 2018 2018
CUI: C0745153
Disease: Hypoglycaemic episode
Hypoglycaemic episode 		disease Disease or Syndrome 8 2 0.010 None 1.000 1 2018 2018
CUI: C0854889
Disease: Pleural mesothelioma malignant advanced
Pleural mesothelioma malignant advanced 		disease Neoplastic Process 8 0.010 None 1.000 1 2019 2019
CUI: C3805156
Disease: Chronic hepatitis C virus genotype 1
Chronic hepatitis C virus genotype 1 		disease Digestive System Diseases; Infections Disease or Syndrome 8 2 0.010 None 1.000 1 2013 2013
CUI: C4722446
Disease: ENCEPHALITIS/ENCEPHALOPATHY, MILD, WITH REVERSIBLE MYELIN VACUOLIZATION
ENCEPHALITIS/ENCEPHALOPATHY, MILD, WITH REVERSIBLE MYELIN VACUOLIZATION 		disease Disease or Syndrome 9 1 0.020 None 1.000 2 2017 2017
CUI: C0155601
Disease: Hypertensive heart and renal disease
Hypertensive heart and renal disease 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases Disease or Syndrome 9 0.010 None 1.000 1 2019 2019
CUI: C0406632
Disease: Autoimmune skin disease
Autoimmune skin disease 		disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 9 0.010 None 1.000 1 2019 2019
CUI: C0276434
Disease: Acute type A viral hepatitis
Acute type A viral hepatitis 		disease Digestive System Diseases; Infections Disease or Syndrome 10 0.010 None 1.000 1 2017 2017
CUI: C0334513
Disease: Sarcomatoid Mesothelioma
Sarcomatoid Mesothelioma 		disease Neoplasms; Respiratory Tract Diseases Neoplastic Process 10 0.010 None 1.000 1 2011 2011
CUI: C0272325
Disease: Factor 8 deficiency, acquired
Factor 8 deficiency, acquired 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 11 0.010 None 1.000 1 2019 2019
CUI: C0729552
Disease: Genital infection
Genital infection 		group Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 11 0.010 None 1.000 1 2017 2017
CUI: C1300257
Disease: Thanatophoric dysplasia, type 2
Thanatophoric dysplasia, type 2 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 11 17 0.010 None 1.000 1 2019 2019
CUI: C1333768
Disease: Gastric Gastrointestinal Stromal Tumor
Gastric Gastrointestinal Stromal Tumor 		disease Digestive System Diseases; Neoplasms Neoplastic Process 11 1 0.010 None 1.000 1 2008 2008
CUI: C0409652
Disease: Seronegative rheumatoid arthritis
Seronegative rheumatoid arthritis 		disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases Disease or Syndrome 12 0.010 None 1.000 1 2019 2019
CUI: C0948775
Disease: High weight
High weight 		phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Sign or Symptom 12 0.010 None 1.000 1 2017 2017
CUI: C0022350
Disease: Jaundice, Chronic Idiopathic
Jaundice, Chronic Idiopathic 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 13 12 0.010 None 1.000 1 1996 1996
CUI: C1761609
Disease: Aspiration pneumonitis
Aspiration pneumonitis 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 13 0.010 None 1.000 1 2020 2020
CUI: C0206675
Disease: Adenomatoid Tumor
Adenomatoid Tumor 		disease Neoplasms Neoplastic Process 14 0.010 None 1.000 1 2007 2007
CUI: C1842090
Disease: Platelet Glycoprotein IV Deficiency
Platelet Glycoprotein IV Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 14 12 0.010 None 1.000 1 2019 2019
CUI: C0343532
Disease: Streptococcal toxic shock syndrome
Streptococcal toxic shock syndrome 		phenotype Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 16 0.010 None 1.000 1 2009 2009