ADM, adrenomedullin, 133

N. diseases: 405; N. variants: 1
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: C0158369
Disease: Swelling of limb
Swelling of limb
phenotype Sign or Symptom 1 0.010 None 1.000 1 2013 2013
CUI: C0694575
Disease: Macular fibrosis
Macular fibrosis
disease Disease or Syndrome 1 0.010 None 1.000 1 2000 2000
CUI: C1401086
Disease: Peripheral Vascular Insufficiency
Peripheral Vascular Insufficiency
disease Cardiovascular Diseases Disease or Syndrome 1 0.010 None 1.000 1 2014 2014
CUI: C0154743
Disease: Ulnar Neuropathies
Ulnar Neuropathies
group Nervous System Diseases Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C0553718
Disease: Renal artery occlusion
Renal artery occlusion
disease Disease or Syndrome 3 0.010 None 1.000 1 2004 2004
CUI: C4721918
Disease: Fibrothecoma
Fibrothecoma
disease Neoplasms Neoplastic Process 3 0.010 None 1.000 1 2009 2009
CUI: C0743323
Disease: Acute dyspnea
Acute dyspnea
phenotype Sign or Symptom 4 0.020 None 1.000 2 2017 2018
CUI: C0035319
Disease: Retinal Necrosis Syndrome, Acute
Retinal Necrosis Syndrome, Acute
disease Eye Diseases Disease or Syndrome 4 0.010 None 1.000 1 2000 2000
CUI: C0149746
Disease: Orthostasis
Orthostasis
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 5 0.010 None 1.000 1 2017 2017
CUI: C0700200
Disease: Presyncope
Presyncope
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 5 0.010 None 1.000 1 2018 2018
CUI: C0740577
Disease: Acute abdominal pain
Acute abdominal pain
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 6 0.010 None 1.000 1 2019 2019
Severe hypoxic ischemic encephalopathy
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 6 0.010 None 1.000 1 2002 2002
CUI: C0238577
Disease: Abdominal wall defect
Abdominal wall defect
group Congenital Abnormality 8 0.010 None 1.000 1 2017 2017
CUI: C0265116
Disease: Chronic cerebral ischemia
Chronic cerebral ischemia
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 8 0.010 None 1.000 1 2014 2014
CUI: C0751887
Disease: Medullary Neoplasms
Medullary Neoplasms
disease Neoplasms; Nervous System Diseases Neoplastic Process 8 0.010 None 1.000 1 1997 1997
CUI: C0038187
Disease: Starvation
Starvation
phenotype Nutritional and Metabolic Diseases Finding 10 0.200 None 1.000 1 2007 2007
CUI: C0265191
Disease: Chronic acquired lymphedema
Chronic acquired lymphedema
disease Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases Disease or Syndrome 12 0.010 None 1.000 1 2013 2013
CUI: C0948268
Disease: Hemodynamic instability
Hemodynamic instability
disease Disease or Syndrome 15 0.010 None 1.000 1 2017 2017
CUI: C1836438
Disease: Familial neurocardiogenic syncope
Familial neurocardiogenic syncope
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 16 1 0.010 None 1.000 1 2019 2019
Primary immunoglobulin A nephropathy (disorder)
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases Disease or Syndrome 16 1 0.010 None 1.000 1 2005 2005
CUI: C0343084
Disease: Capillary Leak Syndrome
Capillary Leak Syndrome
disease Cardiovascular Diseases Disease or Syndrome 18 0.010 None 1.000 1 2018 2018
CUI: C1261287
Disease: Stenosis
Stenosis
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 19 1 0.010 None 1.000 1 2004 2004
CUI: C0149520
Disease: Acute Cholecystitis
Acute Cholecystitis
disease Digestive System Diseases Disease or Syndrome 21 0.010 None 1.000 1 2019 2019
CUI: C0236788
Disease: Bipolar II disorder
Bipolar II disorder
disease Mental Disorders Mental or Behavioral Dysfunction 21 12 0.010 None 1.000 1 2010 2010
CUI: C4551504
Disease: Oculocutaneous albinism type 1A
Oculocutaneous albinism type 1A
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 21 101 0.010 None 1.000 1 2018 2018