PEPD, peptidase D, 5184

N. diseases: 113; N. variants: 36
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: C0268532
Disease: Deficiency of prolidase
Deficiency of prolidase
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 2 12 0.760 strong 1.000 16 12 1990 2017
Diabetes Mellitus, Non-Insulin-Dependent
disease Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 3134 2672 0.430 None 1.000 4 2 2011 2019
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly
phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Finding 523 30 0.400 None 1.000 1 2006 2006
CUI: C0037299
Disease: Skin Ulcer
Skin Ulcer
phenotype Skin and Connective Tissue Diseases Disease or Syndrome 151 1 0.400 None 1.000 1 2006 2006
CUI: C0038002
Disease: Splenomegaly
Splenomegaly
phenotype Pathological Conditions, Signs and Symptoms Finding 345 19 0.400 None 1.000 1 2006 2006
CUI: C3494247
Disease: Organothiophosphonate Poisoning
Organothiophosphonate Poisoning
disease Chemically-Induced Disorders Injury or Poisoning 4 0.300 None 1.000 1 2013 2013
CUI: C3494248
Disease: Organothiophosphate Poisoning
Organothiophosphate Poisoning
disease Chemically-Induced Disorders Injury or Poisoning 4 0.300 None 1.000 1 2013 2013
CUI: C0353676
Disease: Organophosphorus Poisoning
Organophosphorus Poisoning
disease Chemically-Induced Disorders Injury or Poisoning 4 0.300 None 1.000 1 2013 2013
CUI: C3714514
Disease: Infection
Infection
group Infections Pathologic Function 491 0.300 None 1.000 1 2006 2006
CUI: C0700359
Disease: Organophosphate poisoning
Organophosphate poisoning
disease Chemically-Induced Disorders Injury or Poisoning 5 0.300 None 1.000 1 2013 2013
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases
group Respiratory Tract Diseases Disease or Syndrome 198 109 0.300 None 1.000 1 2006 2006
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy
disease Cardiovascular Diseases Disease or Syndrome 560 635 0.200 None 0
Cardiomyopathy, Hypertrophic, Familial
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 83 355 0.200 None 0
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 1883 1172 0.110 None 1.000 1 2007 2007
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
disease Mental or Behavioral Dysfunction 1825 553 0.110 None 1.000 1 2015 2015
High density lipoprotein measurement
phenotype Laboratory Procedure 545 1440 0.100 None 1.000 5 4 2013 2019
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
phenotype Laboratory Procedure 563 1418 0.100 None 1.000 4 3 2013 2019
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
phenotype Organism Attribute 565 1138 0.100 None 1.000 4 2 2015 2019
CUI: C1305855
Disease: Body mass index
Body mass index
phenotype Clinical Attribute 1014 2689 0.100 None 1.000 3 4 2012 2019
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
phenotype Clinical Attribute 843 1931 0.100 None 1.000 2 2 2018 2019
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure
phenotype Diagnostic Procedure 88 252 0.100 None 1.000 2 2 2012 2012
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index
phenotype Finding 88 252 0.100 None 1.000 2 2 2012 2012
CUI: C2700366
Disease: Adiponectin Measurement
Adiponectin Measurement
phenotype Laboratory Procedure 25 70 0.100 None 1.000 2 3 2012 2014
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
disease Mental Disorders Mental or Behavioral Dysfunction 2872 2897 0.100 None 1.000 1 1 2015 2015
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
phenotype Laboratory Procedure 717 1599 0.100 None 1.000 1 1 2019 2019