HAMP, hepcidin antimicrobial peptide, 57817

N. diseases: 377; N. variants: 15
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: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 405 135 0.010 None 1.000 1 2017 2017
CUI: C0041956
Disease: Ureteral obstruction
Ureteral obstruction 		phenotype Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 359 0.010 None 1.000 1 2020 2020
CUI: C0041782
Disease: Deficiency anemias
Deficiency anemias 		group Hemic and Lymphatic Diseases Disease or Syndrome 5 0.010 None 1.000 1 2017 2017
CUI: C0854248
Disease: Pneumonia due to Gram negative bacteria
Pneumonia due to Gram negative bacteria 		group Infections; Respiratory Tract Diseases Disease or Syndrome 9 0.010 None 1.000 1 2017 2017
CUI: C0040149
Disease: Subacute thyroiditis
Subacute thyroiditis 		disease Endocrine System Diseases Disease or Syndrome 13 0.010 None 1.000 1 2019 2019
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm 		disease Neoplasms; Endocrine System Diseases Neoplastic Process 1164 135 0.010 None 1.000 1 2018 2018
CUI: C0040028
Disease: Thrombocythemia, Essential
Thrombocythemia, Essential 		disease Hemic and Lymphatic Diseases Disease or Syndrome 220 37 0.010 None 1.000 1 2013 2013
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction 		phenotype Disease or Syndrome 716 25 0.010 None 1.000 1 2018 2018
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		group Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1658 591 0.010 None 1.000 1 2019 2019
CUI: C0037061
Disease: Siderosis
Siderosis 		disease Respiratory Tract Diseases; Occupational Diseases Disease or Syndrome 23 2 0.010 None 1.000 1 2008 2008
CUI: C0037054
Disease: Sickle Cell Trait
Sickle Cell Trait 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 75 16 0.010 None < 0.001 1 2018 2018
CUI: C0858321
Disease: Plasmodium vivax infection
Plasmodium vivax infection 		disease Infections Disease or Syndrome 21 1 0.010 None 1.000 1 2015 2015
CUI: C0847226
Disease: Viral keratitis
Viral keratitis 		disease Pathological Conditions, Signs and Symptoms; Infections; Eye Diseases Disease or Syndrome 4 0.010 None 1.000 1 2011 2011
CUI: C0042769
Disease: Virus Diseases
Virus Diseases 		group Infections Disease or Syndrome 1471 42 0.010 None 1.000 1 2011 2011
CUI: C0744855
Disease: hepatitis immune
hepatitis immune 		disease Disease or Syndrome 4 0.010 None < 0.001 1 2007 2007
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		disease Cardiovascular Diseases Disease or Syndrome 230 93 0.010 None 1.000 1 2011 2011
CUI: C0149520
Disease: Acute Cholecystitis
Acute Cholecystitis 		disease Digestive System Diseases Disease or Syndrome 21 0.010 None 1.000 1 2011 2011
CUI: C0085762
Disease: Alcohol abuse
Alcohol abuse 		disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 156 24 0.010 None 1.000 1 2012 2012
CUI: C0085693
Disease: Acute appendicitis NOS (disorder)
Acute appendicitis NOS (disorder) 		disease Digestive System Diseases; Infections Disease or Syndrome 43 2 0.010 None 1.000 1 2018 2018
CUI: C0085581
Disease: Restrictive lung disease
Restrictive lung disease 		disease Respiratory Tract Diseases Disease or Syndrome 13 0.010 None 1.000 1 2017 2017
CUI: C0745744
Disease: End Stage Liver Disease
End Stage Liver Disease 		disease Digestive System Diseases Disease or Syndrome 80 3 0.010 None 1.000 1 2015 2015
CUI: C0746102
Disease: Chronic lung disease
Chronic lung disease 		disease Respiratory Tract Diseases Disease or Syndrome 133 12 0.010 None 1.000 1 2012 2012
CUI: C0042870
Disease: Vitamin D Deficiency
Vitamin D Deficiency 		disease Nutritional and Metabolic Diseases Disease or Syndrome 153 37 0.010 None 1.000 1 2017 2017
CUI: C0042847
Disease: Vitamin B 12 Deficiency
Vitamin B 12 Deficiency 		disease Nutritional and Metabolic Diseases Disease or Syndrome 29 11 0.010 None 1.000 1 2017 2017
CUI: C0751202
Disease: Cystathionine beta-Synthase Deficiency Disease
Cystathionine beta-Synthase Deficiency Disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Nervous System Diseases Disease or Syndrome 27 118 0.010 None 1.000 1 2019 2019