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.
Lethal tight skin contracture syndrome (disorder)
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 4 10 0.200 None 1.000 2 2003 2003
CUI: C0276253
Disease: Cytomegaloviral pneumonia
Cytomegaloviral pneumonia
disease Infections; Respiratory Tract Diseases Disease or Syndrome 6 0.010 None 1.000 1 2017 2017
CUI: C1837610
Disease: ICHTHYOSIS PREMATURITY SYNDROME
ICHTHYOSIS PREMATURITY SYNDROME
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 9 6 0.790 None 1.000 10 6 2009 2020
Desquamation of skin soon after birth
phenotype Finding 14 0.100 None 0
CUI: C1504431
Disease: Idiopathic pneumonia syndrome
Idiopathic pneumonia syndrome
disease Infections; Respiratory Tract Diseases Disease or Syndrome 18 0.030 None 1.000 3 2017 2019
CUI: C0011432
Disease: Dentin Sensitivity
Dentin Sensitivity
disease Stomatognathic Diseases Disease or Syndrome 19 0.010 None 1.000 1 2018 2018
Ichthyosiform Erythroderma, Congenital
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 31 11 0.020 None 1.000 2 2012 2013
Congenital Nonbullous Ichthyosiform Erythroderma
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 36 16 0.020 None 1.000 2 2012 2013
Severe Fever with Thrombocytopenia Syndrome
disease Hemic and Lymphatic Diseases Disease or Syndrome 55 1 0.010 None 1.000 1 2018 2018
CUI: C0340076
Disease: Asthmatic pulmonary eosinophilia
Asthmatic pulmonary eosinophilia
disease Respiratory Tract Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 62 1 0.010 None 1.000 1 2017 2017
CUI: C3714619
Disease: Insulin resistance syndrome
Insulin resistance syndrome
disease Nutritional and Metabolic Diseases Disease or Syndrome 62 15 0.010 None 1.000 1 2004 2004
CUI: C4281993
Disease: Neonatal respiratory distress
Neonatal respiratory distress
phenotype Respiratory Tract Diseases Finding 64 34 0.100 None 0
CUI: C0034068
Disease: Pulmonary Eosinophilia
Pulmonary Eosinophilia
disease Respiratory Tract Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 70 1 0.010 None 1.000 1 2017 2017
CUI: C0740380
Disease: Varicella zoster
Varicella zoster
disease Disease or Syndrome 71 2 0.010 None 1.000 1 2017 2017
CUI: C0020758
Disease: Congenital ichthyosis
Congenital ichthyosis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 80 11 0.030 None 1.000 3 2012 2015
CUI: C0015696
Disease: Fatty Liver, Alcoholic
Fatty Liver, Alcoholic
disease Digestive System Diseases; Chemically-Induced Disorders Disease or Syndrome 94 6 0.200 None 1.000 1 2005 2005
CUI: C0011119
Disease: Decompression Sickness
Decompression Sickness
disease Wounds and Injuries Disease or Syndrome 98 0.010 None 1.000 1 2019 2019
CUI: C0037268
Disease: Skin Abnormalities
Skin Abnormalities
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Congenital Abnormality 106 16 0.010 None 1.000 1 2019 2019
CUI: C0006271
Disease: Bronchiolitis
Bronchiolitis
disease Infections; Respiratory Tract Diseases Disease or Syndrome 118 32 0.010 None 1.000 1 2017 2017
Respiratory Distress Syndrome, Newborn
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases Disease or Syndrome 177 37 0.100 None 0
CUI: C0151526
Disease: Premature Birth
Premature Birth
phenotype Female Urogenital Diseases and Pregnancy Complications Pathologic Function 192 50 0.100 None 0
CUI: C0020757
Disease: Ichthyoses
Ichthyoses
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 194 18 0.120 None 1.000 2 2012 2015
CUI: C4317109
Disease: Epileptic Seizures
Epileptic Seizures
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 250 7 0.010 None 1.000 1 2019 2019
CUI: C0027066
Disease: Myoclonus
Myoclonus
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 265 34 0.010 None 1.000 1 2007 2007
CUI: C1333064
Disease: Classical Hodgkin's Lymphoma
Classical Hodgkin's Lymphoma
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 285 20 0.010 None 1.000 1 2020 2020