CPE, carboxypeptidase E, 1363

N. diseases: 101; N. variants: 7
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: C0342283
Disease: Hyperproinsulinemia
Hyperproinsulinemia
disease Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 6 6 0.050 None 1.000 5 1998 2019
CUI: C4330695
Disease: Mitochondrial Diabetes
Mitochondrial Diabetes
disease Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 7 0.010 None 1.000 1 2006 2006
CUI: C0578159
Disease: Antibiotic-associated diarrhea
Antibiotic-associated diarrhea
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 14 0.010 None 1.000 1 2005 2005
CUI: C1704374
Disease: Carcinoma of Endocrine Gland
Carcinoma of Endocrine Gland
disease Neoplasms; Endocrine System Diseases Neoplastic Process 22 0.010 None 1.000 1 2010 2010
CUI: C1290807
Disease: Diarrheal disorder
Diarrheal disorder
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 32 0.010 None 1.000 1 2008 2008
CUI: C0010246
Disease: Coxsackievirus Infections
Coxsackievirus Infections
group Infections Disease or Syndrome 48 1 0.010 None 1.000 1 2017 2017
CUI: C0280232
Disease: stage, cervical cancer
stage, cervical cancer
phenotype Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 48 0.010 None 1.000 1 2016 2016
CUI: C0856727
Disease: Cholesterol gallstones
Cholesterol gallstones
disease Digestive System Diseases Disease or Syndrome 51 12 0.010 None 1.000 1 2016 2016
CUI: C0862506
Disease: Borderline ovarian tumour
Borderline ovarian tumour
disease Neoplastic Process 54 0.010 None 1.000 1 2019 2019
CUI: C0920563
Disease: Insulin Sensitivity
Insulin Sensitivity
phenotype Nutritional and Metabolic Diseases Pathologic Function 62 0.300 None 1.000 1 2004 2004
CUI: C0014130
Disease: Endocrine System Diseases
Endocrine System Diseases
group Endocrine System Diseases Disease or Syndrome 74 0.300 None 1.000 1 2004 2004
Cervical intraepithelial neoplasia grade 1
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 75 1 0.010 None 1.000 1 2016 2016
CUI: C4041080
Disease: Neurocognitive Disorders
Neurocognitive Disorders
group Mental Disorders Mental or Behavioral Dysfunction 79 0.010 None 1.000 1 2019 2019
Delirium, Dementia, Amnestic, Cognitive Disorders
group Mental Disorders Mental or Behavioral Dysfunction 83 0.010 None 1.000 1 2019 2019
CUI: C0017160
Disease: Gastroenteritis
Gastroenteritis
disease Digestive System Diseases Disease or Syndrome 94 0.010 None 1.000 1 2009 2009
CUI: C0206368
Disease: Exfoliation Syndrome
Exfoliation Syndrome
disease Eye Diseases Disease or Syndrome 94 74 0.010 None 1.000 1 2019 2019
CUI: C0040997
Disease: Trigeminal Neuralgia
Trigeminal Neuralgia
disease Nervous System Diseases; Stomatognathic Diseases Disease or Syndrome 107 1 0.010 None 1.000 1 2017 2017
CUI: C0877015
Disease: Pelvic Organ Prolapse
Pelvic Organ Prolapse
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 119 49 0.110 None 1.000 1 1 2015 2015
CUI: C0334299
Disease: Carcinoid tumor no ICD-O subtype
Carcinoid tumor no ICD-O subtype
phenotype Neoplasms Neoplastic Process 122 0.010 None 1.000 1 1988 1988
CUI: C0008055
Disease: Chikungunya Fever
Chikungunya Fever
disease Infections Disease or Syndrome 137 10 0.010 None 1.000 1 2017 2017
CUI: C0017178
Disease: Gastrointestinal Diseases
Gastrointestinal Diseases
group Digestive System Diseases Disease or Syndrome 144 14 0.060 None 1.000 6 2000 2018
CUI: C0021655
Disease: Insulin Resistance
Insulin Resistance
phenotype Nutritional and Metabolic Diseases Pathologic Function 162 53 0.300 None 1.000 1 2004 2004
CUI: C0521707
Disease: Bilateral cataracts (disorder)
Bilateral cataracts (disorder)
disease Eye Diseases Disease or Syndrome 166 37 0.010 None 1.000 1 2009 2009
CUI: C0271623
Disease: Hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism
disease Endocrine System Diseases Disease or Syndrome 178 18 0.010 None 1.000 1 2015 2015
Malformations of Cortical Development, Group II
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality 180 101 0.010 None 1.000 1 2019 2019