GIP, gastric inhibitory polypeptide, 2695

N. diseases: 110; 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.
Other specified diseases of pancreas
group Digestive System Diseases Disease or Syndrome 1 0.200 None 1.000 1 1985 1985
Fetal malnutrition without mention of light-for-dates
disease Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 3 0.010 None 1.000 1 1998 1998
CUI: C0158850
Disease: Fetal Malnutrition
Fetal Malnutrition
disease Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 5 0.010 None 1.000 1 1998 1998
CUI: C4525496
Disease: Hamster Insulinoma
Hamster Insulinoma
disease Neoplastic Process 7 0.010 None 1.000 1 1993 1993
CUI: C2242728
Disease: Cystic fibrosis related diabetes
Cystic fibrosis related diabetes
disease Disease or Syndrome 8 0.010 None 1.000 1 2019 2019
CUI: C0038187
Disease: Starvation
Starvation
phenotype Nutritional and Metabolic Diseases Finding 10 0.200 None 1.000 1 1983 1983
CUI: C0342495
Disease: Macronodular adrenal hyperplasia
Macronodular adrenal hyperplasia
phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 15 0.020 None 1.000 2 1999 2019
CUI: C0206635
Disease: Myelolipoma
Myelolipoma
disease Neoplasms Neoplastic Process 16 1 0.010 None 1.000 1 2019 2019
CUI: C1621895
Disease: Adrenal hyperplasia
Adrenal hyperplasia
disease Pathological Conditions, Signs and Symptoms; Neoplasms; Endocrine System Diseases Disease or Syndrome 33 0.020 None 1.000 2 1999 2005
Acth-Independent Macronodular Adrenal Hyperplasia
disease Endocrine System Diseases Disease or Syndrome 46 8 0.010 None 1.000 1 2004 2004
CUI: C3845502
Disease: Myocardial infarction, stroke
Myocardial infarction, stroke
disease Disease or Syndrome 46 3 0.010 None 1.000 1 2016 2016
CUI: C0149793
Disease: Amaurosis Fugax
Amaurosis Fugax
phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Sign or Symptom 49 2 0.010 None 1.000 1 2016 2016
CUI: C0001622
Disease: Adrenal Gland Hyperfunction
Adrenal Gland Hyperfunction
phenotype Endocrine System Diseases Disease or Syndrome 50 0.010 None 1.000 1 1994 1994
CUI: C1257763
Disease: Overnutrition
Overnutrition
phenotype Nutritional and Metabolic Diseases Disease or Syndrome 54 0.050 None 1.000 5 2003 2019
CUI: C0001618
Disease: Tumors of Adrenal Cortex
Tumors of Adrenal Cortex
group Neoplasms; Endocrine System Diseases Neoplastic Process 74 5 0.010 None 1.000 1 1998 1998
CUI: C0267963
Disease: Exocrine pancreatic insufficiency
Exocrine pancreatic insufficiency
disease Digestive System Diseases Disease or Syndrome 82 26 0.010 None 1.000 1 2018 2018
CUI: C0020428
Disease: Hyperaldosteronism
Hyperaldosteronism
disease Endocrine System Diseases Disease or Syndrome 84 6 0.010 None 1.000 1 2017 2017
CUI: C0001627
Disease: Congenital adrenal hyperplasia
Congenital adrenal hyperplasia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 87 36 0.020 None 1.000 2 1999 2005
CUI: C0948379
Disease: Impaired insulin secretion
Impaired insulin secretion
disease Disease or Syndrome 88 14 0.010 None 1.000 1 1996 1996
Heart failure with preserved ejection fraction [HFpEF]
disease Disease or Syndrome 89 4 0.010 None 1.000 1 2018 2018
CUI: C0917805
Disease: Transient Cerebral Ischemia
Transient Cerebral Ischemia
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 98 9 0.010 None 1.000 1 2016 2016
Maturity onset diabetes mellitus in young
disease Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 105 49 0.010 None 1.000 1 2012 2012
Pituitary-dependent Cushing's disease
disease Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 115 8 0.020 None 1.000 2 2005 2005
CUI: C2931689
Disease: Dystrophia myotonica 2
Dystrophia myotonica 2
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 118 21 0.010 None 1.000 1 2019 2019
CUI: C0342443
Disease: Adrenal Cushing's syndrome
Adrenal Cushing's syndrome
disease Endocrine System Diseases Disease or Syndrome 120 9 0.100 None 1.000 17 1996 2019