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: C1142276
Disease: Renal anemia
Renal anemia 		disease Disease or Syndrome 12 0.030 None 1.000 3 2004 2017
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease 		disease Disease or Syndrome 741 81 0.030 None 1.000 3 2012 2017
CUI: C0268070
Disease: Hypocupremia
Hypocupremia 		disease Disease or Syndrome 23 2 0.020 None 1.000 2 2006 2017
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		phenotype Laboratory Procedure 593 988 0.100 None 1.000 2 3 2017 2019
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		phenotype Neoplastic Process 6626 169 0.020 None 1.000 2 2008 2018
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		phenotype Laboratory or Test Result 593 988 0.100 None 1.000 2 3 2017 2019
CUI: C2750440
Disease: FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 1
FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 1 		disease Finding 63 2 0.200 None 1.000 2 2017 2018
CUI: C2750441
Disease: LIVER DISEASE, ALCOHOLIC, SUSCEPTIBILITY TO, 1
LIVER DISEASE, ALCOHOLIC, SUSCEPTIBILITY TO, 1 		phenotype Finding 63 0.200 None 1.000 2 2017 2018
CUI: C3150651
Disease: FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 2
FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 2 		phenotype Finding 63 0.200 None 1.000 2 2017 2018
CUI: C3160718
Disease: PARKINSON DISEASE, LATE-ONSET
PARKINSON DISEASE, LATE-ONSET 		disease Disease or Syndrome 247 76 0.020 None 1.000 2 2019 2020
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		disease Neoplastic Process 3669 502 0.020 None 0.500 2 2008 2017
CUI: C0221106
Disease: Alkalemia
Alkalemia 		disease Disease or Syndrome 38 0.010 None 1.000 1 2013 2013
CUI: C0240225
Disease: Liver mass
Liver mass 		phenotype Disease or Syndrome 36 0.010 None 1.000 1 2016 2016
CUI: C0699753
Disease: Cancer Relapse
Cancer Relapse 		disease Neoplastic Process 48 0.010 None 1.000 1 2019 2019
CUI: C0740989
Disease: Chronic iron deficiency anaemia
Chronic iron deficiency anaemia 		disease Disease or Syndrome 2 0.010 None 1.000 1 2010 2010
CUI: C0744855
Disease: hepatitis immune
hepatitis immune 		disease Disease or Syndrome 4 0.010 None < 0.001 1 2007 2007
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction 		phenotype Disease or Syndrome 716 25 0.010 None 1.000 1 2018 2018
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		phenotype Finding 653 1206 0.100 None 1.000 1 1 2019 2019
CUI: C1735608
Disease: SLE flare
SLE flare 		disease Disease or Syndrome 5 0.010 None < 0.001 1 2017 2017
CUI: C3826743
Disease: Anemia in children
Anemia in children 		disease Disease or Syndrome 9 0.010 None 1.000 1 2018 2018
CUI: C0241013
Disease: Increased serum ferritin
Increased serum ferritin 		phenotype Finding 23 1 0.100 None 0
CUI: C1848701
Disease: Elevated hepatic transaminase
Elevated hepatic transaminase 		phenotype Finding 212 9 0.100 None 0
CUI: C4022892
Disease: Elevated transferrin saturation
Elevated transferrin saturation 		phenotype Finding 3 0.100 None 0
CUI: C4023047
Disease: Abnormality of endocrine pancreas physiology
Abnormality of endocrine pancreas physiology 		phenotype Pathologic Function 4 0.100 None 0
CUI: C4023583
Disease: Abnormality of iron homeostasis
Abnormality of iron homeostasis 		phenotype Finding 5 1 0.100 None 0