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: C0021368
Disease: Inflammation
Inflammation
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 467 0.300 None 1.000 1 2010 2010
CUI: C0085129
Disease: Bronchial Hyperreactivity
Bronchial Hyperreactivity
disease Respiratory Tract Diseases Disease or Syndrome 112 18 0.300 None 1.000 1 2009 2009
CUI: C0751407
Disease: Pain, Migratory
Pain, Migratory
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 50 0.300 None 1.000 1 2010 2010
CUI: C0751408
Disease: Suffering, Physical
Suffering, Physical
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 50 0.300 None 1.000 1 2010 2010
CUI: C0234238
Disease: Ache
Ache
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 50 0.300 None 1.000 1 2010 2010
CUI: C0458259
Disease: Pain, Crushing
Pain, Crushing
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 50 0.300 None 1.000 1 2010 2010
CUI: C0458257
Disease: Pain, Splitting
Pain, Splitting
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 50 0.300 None 1.000 1 2010 2010
CUI: C0234254
Disease: Radiating pain
Radiating pain
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 51 0.300 None 1.000 1 2010 2010
CUI: C0234230
Disease: Pain, Burning
Pain, Burning
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 56 0.300 None 1.000 1 2010 2010
CUI: C0037383
Disease: Sneezing
Sneezing
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 21 2 0.300 None 1.000 1 2017 2017
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 302 18 0.200 None 1.000 1 2014 2014
CUI: C0234245
Disease: Visceral Pain
Visceral Pain
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 58 0.200 None 1.000 1 2013 2013
CUI: C3489856
Disease: Cold Hypersensitivity
Cold Hypersensitivity
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 12 0.200 None 1.000 1 2010 2010
CUI: C0154723
Disease: Migraine with Aura
Migraine with Aura
disease Nervous System Diseases Disease or Syndrome 87 56 0.010 None 1.000 1 2018 2018
CUI: C0175694
Disease: Smith-Lemli-Opitz Syndrome
Smith-Lemli-Opitz Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 30 96 0.010 None 1.000 1 2017 2017
CUI: C0178422
Disease: Cramp in foot
Cramp in foot
phenotype Sign or Symptom 1 0.010 None 1.000 1 2017 2017
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
phenotype Pathological Conditions, Signs and Symptoms Neoplastic Process 3865 72 0.010 None 1.000 1 2014 2014
CUI: C0521585
Disease: Gastrointestinal mucositis
Gastrointestinal mucositis
disease Digestive System Diseases; Stomatognathic Diseases Disease or Syndrome 98 19 0.010 None 1.000 1 2017 2017
CUI: C0206139
Disease: Lichen Planus, Oral
Lichen Planus, Oral
disease Skin and Connective Tissue Diseases; Stomatognathic Diseases Disease or Syndrome 257 20 0.010 None 1.000 1 2017 2017
Metastatic malignant neoplasm to brain
disease Pathological Conditions, Signs and Symptoms; Neoplasms; Nervous System Diseases Neoplastic Process 392 28 0.010 None 1.000 1 2017 2017
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
disease Neoplasms Neoplastic Process 2438 563 0.010 None 1.000 1 2017 2017
CUI: C0035335
Disease: Retinoblastoma
Retinoblastoma
disease Neoplasms; Eye Diseases Neoplastic Process 853 193 0.010 None 1.000 1 2012 2012
CUI: C0036280
Disease: Burn scar
Burn scar
disease Pathological Conditions, Signs and Symptoms; Wounds and Injuries Acquired Abnormality 11 0.010 None 1.000 1 2015 2015
CUI: C0037284
Disease: Skin lesion
Skin lesion
group Skin and Connective Tissue Diseases Disease or Syndrome 563 52 0.010 None 1.000 1 2015 2015
CUI: C0042963
Disease: Vomiting
Vomiting
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 303 23 0.010 None 1.000 1 2017 2017