PGPEP1, pyroglutamyl-peptidase I, 54858

N. diseases: 116; N. variants: 8
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.
PHENCYCLIDINE/ARYLCYCLOHEXYLAMINE ABUSE
disease Mental or Behavioral Dysfunction 3 0.010 None 1.000 1 2017 2017
Digestive System Non-Hodgkin Lymphoma
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 3 0.010 None 1.000 1 2018 2018
CUI: C0426359
Disease: Urinary symptoms
Urinary symptoms
phenotype Sign or Symptom 10 0.010 None 1.000 1 2019 2019
CUI: C0694571
Disease: extranodal lymphoma
extranodal lymphoma
disease Neoplastic Process 17 1 0.010 None 1.000 1 2018 2018
CUI: C0851886
Disease: Pneumocystis Infections
Pneumocystis Infections
group Infections Disease or Syndrome 18 0.010 None 1.000 1 2004 2004
CUI: C0742132
Disease: cervical cancer metastasis
cervical cancer metastasis
disease Neoplastic Process 35 0.010 None 1.000 1 2017 2017
CUI: C0152426
Disease: Craniorachischisis
Craniorachischisis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality 38 0.020 None 1.000 2 2011 2012
CUI: C0020256
Disease: Congenital Hydrocephalus
Congenital Hydrocephalus
disease Nervous System Diseases Congenital Abnormality 39 0.010 None 1.000 1 2019 2019
CUI: C0398625
Disease: Protein C Deficiency
Protein C Deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 43 14 0.010 None 1.000 1 2000 2000
CUI: C0149725
Disease: Lower respiratory tract infection
Lower respiratory tract infection
group Infections; Respiratory Tract Diseases Disease or Syndrome 63 7 0.010 None 1.000 1 2008 2008
CUI: C0431128
Disease: Papillary craniopharyngioma
Papillary craniopharyngioma
disease Neoplasms Neoplastic Process 65 2 0.040 None 1.000 4 2001 2019
CUI: C0003175
Disease: Anthrax disease
Anthrax disease
disease Infections Disease or Syndrome 66 3 0.010 None 1.000 1 2019 2019
CUI: C3496069
Disease: cocaine use
cocaine use
disease Mental or Behavioral Dysfunction 67 8 0.010 None 1.000 1 2017 2017
CUI: C0032326
Disease: Pneumothorax
Pneumothorax
phenotype Respiratory Tract Diseases Disease or Syndrome 69 3 0.010 None 1.000 1 2019 2019
CUI: C0021167
Disease: Incontinence
Incontinence
disease Nervous System Diseases Disease or Syndrome 70 1 0.010 None 1.000 1 2017 2017
CUI: C0037090
Disease: Signs and Symptoms, Respiratory
Signs and Symptoms, Respiratory
group Pathological Conditions, Signs and Symptoms Sign or Symptom 73 10 0.010 None 1.000 1 1993 1993
CUI: C0042025
Disease: Urinary Stress Incontinence
Urinary Stress Incontinence
disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 79 5 0.030 None 1.000 3 2017 2020
CUI: C0584960
Disease: Factor V Leiden mutation
Factor V Leiden mutation
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 86 46 0.010 None 1.000 1 2000 2000
CUI: C0035439
Disease: Rheumatic Heart Disease
Rheumatic Heart Disease
disease Infections; Cardiovascular Diseases Disease or Syndrome 102 33 0.010 None < 0.001 1 1998 1998
CUI: C0149745
Disease: Oral Ulcer
Oral Ulcer
disease Stomatognathic Diseases Disease or Syndrome 104 101 0.100 None 1.000 1 1 2019 2019
CUI: C0151514
Disease: Atrophic condition of skin
Atrophic condition of skin
group Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 111 4 0.010 None 1.000 1 2008 2008
CUI: C0751213
Disease: Tactile Allodynia
Tactile Allodynia
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 114 0.010 None 1.000 1 2020 2020
CUI: C1963943
Disease: Atherothrombosis
Atherothrombosis
disease Acquired Abnormality 115 15 0.020 None 1.000 2 2007 2010
CUI: C0497169
Disease: hiv-infection/aids
hiv-infection/aids
disease Infections Disease or Syndrome 124 4 0.010 None 1.000 1 2019 2019
CUI: C0008031
Disease: Chest Pain
Chest Pain
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 154 7 0.010 None 1.000 1 2014 2014