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: C1266002
Disease: Non-small cell carcinoma
Non-small cell carcinoma
disease Neoplasms Neoplastic Process 33 0.010 None 1.000 1 2011 2011
CUI: C0038506
Disease: Stuttering
Stuttering
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Mental or Behavioral Dysfunction 34 8 0.010 None 1.000 1 2017 2017
CUI: C0751074
Disease: Diabetic Neuralgia
Diabetic Neuralgia
disease Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 36 0.030 None 1.000 3 2019 2020
CUI: C1386048
Disease: Intrauterine retardation
Intrauterine retardation
phenotype Pathologic Function 41 56 0.100 None 0 1
CUI: C1960870
Disease: Transformed migraine
Transformed migraine
disease Nervous System Diseases Disease or Syndrome 43 1 0.010 None 1.000 1 2018 2018
Anti-N-Methyl-D-Aspartate Receptor Encephalitis
disease Neoplasms; Immune System Diseases; Nervous System Diseases Disease or Syndrome 43 0.010 None 1.000 1 2019 2019
CUI: C0026552
Disease: Morphine Dependence
Morphine Dependence
disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 44 0.010 None 1.000 1 2017 2017
CUI: C0032051
Disease: Placental Insufficiency
Placental Insufficiency
disease Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 45 0.200 None 1.000 1 2009 2009
CUI: C2985290
Disease: Fetal Alcohol Spectrum Disorders
Fetal Alcohol Spectrum Disorders
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Chemically-Induced Disorders Disease or Syndrome; Congenital Abnormality 46 2 0.200 None 1.000 2 2012 2013
CUI: C0023186
Disease: Learning Disorders
Learning Disorders
group Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders Mental or Behavioral Dysfunction 46 1 0.010 None 1.000 1 2016 2016
CUI: C0795864
Disease: Smith-Magenis syndrome
Smith-Magenis syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 47 8 0.010 None 1.000 1 2014 2014
CUI: C0920299
Disease: Overriding toe
Overriding toe
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Anatomical Abnormality 47 13 0.100 None 0 1
CUI: C0233844
Disease: Clumsiness
Clumsiness
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders Sign or Symptom 48 3 0.100 None 0 1
CUI: C0241074
Disease: Hyperextensible skin
Hyperextensible skin
phenotype Finding 50 11 0.100 None 0 1
CUI: C4317146
Disease: Acid reflux
Acid reflux
phenotype Finding 50 58 0.100 None 0 1
CUI: C0564567
Disease: Impulsive character (finding)
Impulsive character (finding)
phenotype Mental or Behavioral Dysfunction 52 19 0.010 None 1.000 1 2018 2018
CUI: C0242184
Disease: Hypoxia
Hypoxia
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 59 0.200 None 1.000 1 2014 2014
Malformations of Cortical Development
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 60 5 0.010 None 1.000 1 2004 2004
CUI: C2243051
Disease: Large head (disorder)
Large head (disorder)
phenotype Finding 64 116 0.100 None 0 1
Depressive Disorder, Treatment-Resistant
disease Mental Disorders Mental or Behavioral Dysfunction 66 19 0.020 None 1.000 2 1 2014 2017
CUI: C0424101
Disease: Inattention
Inattention
phenotype Mental or Behavioral Dysfunction 66 22 0.010 None 1.000 1 1 2017 2017
Disruptive, Impulse Control, and Conduct Disorders
group Mental Disorders Mental or Behavioral Dysfunction 67 9 0.020 None 1.000 2 2013 2016
CUI: C0236663
Disease: Alcohol withdrawal syndrome
Alcohol withdrawal syndrome
disease Chemically-Induced Disorders; Mental Disorders Disease or Syndrome 67 6 0.020 None 1.000 2 1 2009 2017
CUI: C0683322
Disease: Mental impairment
Mental impairment
disease Mental or Behavioral Dysfunction 67 14 0.110 None 1.000 1 2 2019 2019
CUI: C0239137
Disease: Coxa valga
Coxa valga
phenotype Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Finding 68 5 0.100 None 0 1