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: C0043346
Disease: Xeroderma Pigmentosum
Xeroderma Pigmentosum
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Congenital Abnormality 137 35 0.010 None 1.000 1 2014 2014
CUI: C0240953
Disease: Winged scapula
Winged scapula
phenotype Finding 73 3 0.100 None 0
CUI: C1827524
Disease: Wide spaced nipples
Wide spaced nipples
phenotype Finding 96 19 0.100 None 0 1
CUI: C1849667
Disease: Wide nasal base
Wide nasal base
phenotype Finding 12 3 0.100 None 0 1
Well Differentiated Oligodendroglioma
disease Neoplasms Neoplastic Process 270 22 0.060 None 1.000 6 2 2012 2019
CUI: C0024419
Disease: Waldenstrom Macroglobulinemia
Waldenstrom Macroglobulinemia
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Neoplastic Process 162 15 0.010 None 1.000 1 2 2016 2016
CUI: C0042963
Disease: Vomiting
Vomiting
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 303 23 0.100 None 0
CUI: C0521698
Disease: Vogt-Koyanagi-Harada like syndrome
Vogt-Koyanagi-Harada like syndrome
disease Eye Diseases Disease or Syndrome 4 0.010 None 1.000 1 2018 2018
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
disease Skin and Connective Tissue Diseases Disease or Syndrome 302 92 0.030 None 1.000 3 2015 2019
CUI: C0042900
Disease: Vitiligo
Vitiligo
disease Skin and Connective Tissue Diseases Disease or Syndrome 395 249 0.030 None 1.000 3 2015 2019
CUI: C0042834
Disease: Vital capacity
Vital capacity
phenotype Clinical Attribute 430 746 0.100 None 1.000 1 1 2019 2019
CUI: C0796418
Disease: Visual Pathway Glioma
Visual Pathway Glioma
disease Neoplasms Neoplastic Process 10 0.010 None 1.000 1 2017 2017
CUI: C0042571
Disease: Vertigo
Vertigo
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Sign or Symptom 173 35 0.100 None 0 1
CUI: C4049491
Disease: Verrucous keratosis
Verrucous keratosis
disease Disease or Syndrome 1 0.010 None 1.000 1 2013 2013
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 426 87 0.100 None 0 1
CUI: C0340279
Disease: Ventricular hypertrophy
Ventricular hypertrophy
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 60 9 0.100 None 0 1
CUI: C1402315
Disease: Vascular lesions
Vascular lesions
disease Disease or Syndrome 111 9 0.010 None 1.000 1 2 2019 2019
CUI: C0158570
Disease: Vascular anomaly
Vascular anomaly
phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Anatomical Abnormality 47 5 0.010 None 1.000 1 2018 2018
CUI: C0042164
Disease: Uveitis
Uveitis
disease Eye Diseases Disease or Syndrome 247 43 0.010 None 1.000 1 2018 2018
CUI: C0220633
Disease: Uveal melanoma
Uveal melanoma
disease Neoplasms; Eye Diseases Neoplastic Process 376 22 0.100 None 0.920 25 3 2003 2020
CUI: C2931202
Disease: Urachal cancer
Urachal cancer
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 19 0.010 None 1.000 1 2016 2016
CUI: C2931201
Disease: Urachal adenocarcinoma
Urachal adenocarcinoma
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 2 0.010 None 1.000 1 2014 2014
CUI: C4725093
Disease: Unresectable Melanoma
Unresectable Melanoma
disease Neoplasms Neoplastic Process 7 3 0.060 None 1.000 6 3 2013 2019
CUI: C0457521
Disease: Unicystic ameloblastoma
Unicystic ameloblastoma
disease Neoplasms Neoplastic Process 9 4 0.010 None 1.000 1 2 2019 2019
CUI: C0205698
Disease: Undifferentiated carcinoma
Undifferentiated carcinoma
disease Neoplasms Neoplastic Process 283 8 0.080 None 0.875 8 2 2004 2016