IAPP, islet amyloid polypeptide, 3375

N. diseases: 183; N. variants: 3
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: C0856874
Disease: Subclinical diabetes
Subclinical diabetes
disease Disease or Syndrome 2 0.010 None 1.000 1 2018 2018
CUI: C3534591
Disease: Diabetic Heart Disease
Diabetic Heart Disease
disease Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 4 0.010 None 1.000 1 2014 2014
CUI: C3554225
Disease: LEPTIN RECEPTOR DEFICIENCY
LEPTIN RECEPTOR DEFICIENCY
disease Disease or Syndrome 9 3 0.010 None 1.000 1 2018 2018
CUI: C0341862
Disease: Hypothalamic amenorrhea
Hypothalamic amenorrhea
disease Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 10 2 0.010 None 1.000 1 2008 2008
CUI: C0393735
Disease: Headache Disorders
Headache Disorders
group Nervous System Diseases Disease or Syndrome 14 0.010 None < 0.001 1 2017 2017
Lymphoproliferative Syndrome, X-Linked, 2
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 14 13 0.010 None 1.000 1 2018 2018
CUI: C0265344
Disease: Donohue Syndrome
Donohue Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Endocrine System Diseases Disease or Syndrome 15 22 0.010 None 1.000 1 2018 2018
CUI: C2242710
Disease: Intra-Abdominal Hypertension
Intra-Abdominal Hypertension
disease Musculoskeletal Diseases; Cardiovascular Diseases Disease or Syndrome 17 0.010 None 1.000 1 2018 2018
Pancreatic Intraepithelial Neoplasia-3
disease Neoplastic Process 19 0.010 None 1.000 1 2010 2010
CUI: C0035585
Disease: Rickettsia Infections
Rickettsia Infections
group Infections Disease or Syndrome 22 0.010 None 1.000 1 2017 2017
CUI: C0017689
Disease: Glucagonoma
Glucagonoma
disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 23 1 0.010 None 1.000 1 1991 1991
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type III
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 28 24 0.010 None 1.000 1 2003 2003
CUI: C0032320
Disease: Pneumoperitoneum
Pneumoperitoneum
disease Digestive System Diseases Disease or Syndrome 28 0.010 None 1.000 1 2018 2018
CUI: C0268407
Disease: Senile cardiac amyloidosis
Senile cardiac amyloidosis
disease Nutritional and Metabolic Diseases; Cardiovascular Diseases Disease or Syndrome 33 19 0.010 None 1.000 1 2018 2018
Recurrent Childhood Acute Lymphoblastic Leukemia
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 37 0.010 None 1.000 1 2012 2012
CUI: C2718001
Disease: Protein Misfolding Disorders
Protein Misfolding Disorders
disease Nutritional and Metabolic Diseases Disease or Syndrome 38 1 0.020 None 1.000 2 2017 2018
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis
disease Nutritional and Metabolic Diseases Disease or Syndrome 38 10 0.010 None 1.000 1 2011 2011
CUI: C0221014
Disease: Reactive systemic amyloidosis
Reactive systemic amyloidosis
disease Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 41 11 0.010 None 1.000 1 2011 2011
CUI: C0848332
Disease: Spots on skin
Spots on skin
phenotype Skin and Connective Tissue Diseases Sign or Symptom 43 0.010 None 1.000 1 2017 2017
CUI: C2931038
Disease: Pancreatic carcinoma, familial
Pancreatic carcinoma, familial
disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 43 9 0.010 None 1.000 1 2008 2008
CUI: C2609129
Disease: Autoimmune pancreatitis
Autoimmune pancreatitis
disease Digestive System Diseases; Immune System Diseases Disease or Syndrome 49 3 0.010 None 1.000 1 2010 2010
CUI: C0020175
Disease: Hunger
Hunger
phenotype Behavior and Behavior Mechanisms Sign or Symptom 70 12 0.010 None 1.000 1 2018 2018
CUI: C0234119
Disease: Neuromuscular inhibition
Neuromuscular inhibition
disease Disease or Syndrome 72 2 0.010 None 1.000 1 1991 1991
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 74 68 0.010 None 1.000 1 2018 2018
CUI: C1561826
Disease: Overweight and obesity
Overweight and obesity
disease Disease or Syndrome 81 29 0.010 None 1.000 1 2019 2019