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: C0342326
Disease: Tumor-induced hypoglycemia
Tumor-induced hypoglycemia
disease Disease or Syndrome 4 0.010 None 1.000 1 2015 2015
Miller-McKusick-Malvaux-Syndrome (3M Syndrome)
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 11 11 0.010 None 1.000 1 2010 2010
CUI: C0265449
Disease: Pallister-Killian syndrome
Pallister-Killian syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 12 0.010 None 1.000 1 2015 2015
Secondary malignant neoplasm of female breast
disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 14 1 0.010 None 1.000 1 2018 2018
CUI: C0013403
Disease: Dysplastic Nevus Syndrome
Dysplastic Nevus Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms Neoplastic Process 15 0.010 None 1.000 1 2003 2003
CUI: C0520678
Disease: Postpartum psychosis
Postpartum psychosis
disease Mental Disorders Mental or Behavioral Dysfunction 19 0.010 None 1.000 1 2005 2005
CUI: C0017411
Disease: Female Genital Diseases
Female Genital Diseases
group Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 21 3 0.010 None 1.000 1 2006 2006
CUI: C1332200
Disease: Adult Diffuse Astrocytoma
Adult Diffuse Astrocytoma
disease Neoplasms Neoplastic Process 21 2 0.010 None 1.000 1 2010 2010
CUI: C3899668
Disease: Childhood Diffuse Astrocytoma
Childhood Diffuse Astrocytoma
disease Neoplasms Neoplastic Process 21 2 0.010 None 1.000 1 2010 2010
Primary pigmented nodular adrenocortical disease
disease Disease or Syndrome 22 1 0.010 None 1.000 1 2007 2007
CUI: C3899649
Disease: Childhood Oligoastrocytoma
Childhood Oligoastrocytoma
disease Neoplasms Neoplastic Process 23 3 0.010 None 1.000 1 2011 2011
CUI: C0936016
Disease: Testicular Feminization
Testicular Feminization
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 24 7 0.020 None 1.000 2 2001 2003
CUI: C0024586
Disease: Malignant Carcinoid Syndrome
Malignant Carcinoid Syndrome
disease Neoplasms Disease or Syndrome 25 0.010 None 1.000 1 2000 2000
CUI: C1704417
Disease: Hyperlipoproteinemia Type IIb
Hyperlipoproteinemia Type IIb
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 25 16 0.010 None 1.000 1 1991 1991
CUI: C0280793
Disease: Mixed Oligodendroglioma-Astrocytoma
Mixed Oligodendroglioma-Astrocytoma
disease Neoplasms Neoplastic Process 28 3 0.010 None 1.000 1 2011 2011
CUI: C0280790
Disease: Adult Anaplastic Oligodendroglioma
Adult Anaplastic Oligodendroglioma
disease Neoplasms Neoplastic Process 29 4 0.010 None 1.000 1 2009 2009
Childhood Anaplastic Oligodendroglioma
disease Neoplasms Neoplastic Process 29 4 0.010 None 1.000 1 2009 2009
Left ventricular diastolic dysfunction
disease Cardiovascular Diseases Disease or Syndrome 31 1 0.010 None 1.000 1 2017 2017
Primary Pigmented Nodular Adrenal Dysplasia
disease Congenital Abnormality 31 1 0.010 None 1.000 1 2007 2007
CUI: C0027658
Disease: Neoplasms, Germ Cell and Embryonal
Neoplasms, Germ Cell and Embryonal
group Neoplasms Neoplastic Process 34 0.010 None 1.000 1 2008 2008
CUI: C0238348
Disease: Squamous cell carcinoma of penis
Squamous cell carcinoma of penis
disease Neoplasms; Male Urogenital Diseases Neoplastic Process 40 2 0.010 None 1.000 1 2019 2019
CUI: C0243066
Disease: Atresia
Atresia
disease Congenital Abnormality 44 1 0.010 None 1.000 1 2018 2018
CUI: C0242706
Disease: Hyperoxia
Hyperoxia
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 50 0.200 None 1.000 1 2006 2006
CUI: C1392786
Disease: Cognitive changes
Cognitive changes
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Mental or Behavioral Dysfunction 50 15 0.010 None 1.000 1 2015 2015
CUI: C0008928
Disease: Cleidocranial Dysplasia
Cleidocranial Dysplasia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 52 22 0.010 None 1.000 1 2018 2018