GAST, gastrin, 2520

N. diseases: 236; N. variants: 0
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: C1709246
Disease: Non-Neoplastic Disorder
Non-Neoplastic Disorder 		disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 50 0.010 None 1.000 1 1990 1990
CUI: C0025568
Disease: Metaplasia
Metaplasia 		phenotype Pathological Conditions, Signs and Symptoms Cell or Molecular Dysfunction 52 0.020 None 1.000 2 2003 2004
CUI: C1258085
Disease: Barrett Epithelium
Barrett Epithelium 		disease Digestive System Diseases; Neoplasms Disease or Syndrome 52 0.300 None 1.000 1 2004 2004
CUI: C0151636
Disease: Premature ventricular contractions
Premature ventricular contractions 		phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 56 13 0.010 None 1.000 1 2017 2017
CUI: C0013395
Disease: Dyspepsia
Dyspepsia 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 61 5 0.040 None 0.750 4 1980 2017
CUI: C0025037
Disease: Meckel Diverticulum
Meckel Diverticulum 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Congenital Abnormality 63 0.010 None 1.000 1 2017 2017
CUI: C0027662
Disease: Multiple Endocrine Neoplasia
Multiple Endocrine Neoplasia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases Neoplastic Process 65 11 0.020 None 1.000 2 1994 1996
CUI: C0003175
Disease: Anthrax disease
Anthrax disease 		disease Infections Disease or Syndrome 66 3 0.010 None 1.000 1 2016 2016
CUI: C0221026
Disease: X-linked agammaglobulinemia
X-linked agammaglobulinemia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 68 69 0.010 None 1.000 1 1988 1988
CUI: C0426576
Disease: Gastrointestinal symptom
Gastrointestinal symptom 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 69 7 0.010 None 1.000 1 2020 2020
CUI: C0038354
Disease: Stomach Diseases
Stomach Diseases 		group Digestive System Diseases Disease or Syndrome 70 3 0.010 None 1.000 1 2017 2017
CUI: C0677659
Disease: Gastro-esophageal reflux disease with esophagitis
Gastro-esophageal reflux disease with esophagitis 		disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 71 3 0.020 None 1.000 2 2005 2018
CUI: C0004997
Disease: Benign Ovarian Neoplasm
Benign Ovarian Neoplasm 		disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Neoplastic Process 72 0.010 None 1.000 1 1993 1993
CUI: C0037278
Disease: Skin Diseases, Infectious
Skin Diseases, Infectious 		group Infections; Skin and Connective Tissue Diseases Disease or Syndrome 74 0.020 None 1.000 2 2018 2019
CUI: C0086438
Disease: Hypogammaglobulinemia
Hypogammaglobulinemia 		disease Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 76 2 0.010 None 1.000 1 1988 1988
CUI: C0085437
Disease: Meningitis, Bacterial
Meningitis, Bacterial 		group Infections; Nervous System Diseases Disease or Syndrome 81 16 0.010 None 1.000 1 2013 2013
CUI: C3469186
Disease: HEMOCHROMATOSIS, TYPE 1
HEMOCHROMATOSIS, TYPE 1 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 83 62 0.010 None 1.000 1 2006 2006
CUI: C0014869
Disease: Peptic Esophagitis
Peptic Esophagitis 		disease Digestive System Diseases Disease or Syndrome 85 3 0.020 None 1.000 2 2005 2018
CUI: C0038826
Disease: Superinfection
Superinfection 		group Infections Disease or Syndrome 85 0.010 None 1.000 1 2018 2018
CUI: C0346627
Disease: Intestinal Cancer
Intestinal Cancer 		disease Digestive System Diseases; Neoplasms Neoplastic Process 89 0.010 None 1.000 1 1997 1997
CUI: C0018995
Disease: Hemochromatosis
Hemochromatosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 93 45 0.010 None 1.000 1 2006 2006
CUI: C0035436
Disease: Rheumatic Fever
Rheumatic Fever 		disease Infections; Musculoskeletal Diseases Disease or Syndrome 94 5 0.050 None 1.000 5 2006 2020
CUI: C0549523
Disease: Oropharynx (excludes nasopharynx)
Oropharynx (excludes nasopharynx) 		disease Disease or Syndrome 94 5 0.020 None 1.000 2 2019 2019
CUI: C0001144
Disease: Acne Vulgaris
Acne Vulgaris 		disease Skin and Connective Tissue Diseases Disease or Syndrome 94 37 0.010 None < 0.001 1 2018 2018
CUI: C0000833
Disease: Abscess
Abscess 		phenotype Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 96 1 0.020 None 1.000 2 2016 2019