PEPD, peptidase D, 5184

N. diseases: 11; N. variants: 36
Source: CURATED ×
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 1 12 0.760 strong 1.000 9 12 1990 2017
Diabetes Mellitus, Non-Insulin-Dependent
disease Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 221 1232 0.430 None 1.000 1 2 2011 2019
CUI: C0037299
Disease: Skin Ulcer
Skin Ulcer
phenotype Skin and Connective Tissue Diseases Disease or Syndrome 4 1 0.400 None 1.000 1 2006 2006
CUI: C0038002
Disease: Splenomegaly
Splenomegaly
phenotype Pathological Conditions, Signs and Symptoms Finding 22 19 0.400 None 1.000 1 2006 2006
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly
phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Finding 54 30 0.400 None 1.000 1 2006 2006
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases
group Respiratory Tract Diseases Disease or Syndrome 6 109 0.300 None 1.000 1 2006 2006
CUI: C0353676
Disease: Organophosphorus Poisoning
Organophosphorus Poisoning
disease Chemically-Induced Disorders Injury or Poisoning 4 0.300 None 1.000 1 2013 2013
CUI: C0700359
Disease: Organophosphate poisoning
Organophosphate poisoning
disease Chemically-Induced Disorders Injury or Poisoning 4 0.300 None 1.000 1 2013 2013
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: C3714514
Disease: Infection
Infection
group Infections Pathologic Function 7 0.300 None 1.000 1 2006 2006