Source: BEFREE

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
C0235950 Zinc deficiency disease Nutritional and Metabolic Diseases Disease or Syndrome 89 4
C0043144 Wheezing phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom Abnormality of the respiratory system 127 54
C0043119 Werner Syndrome disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome genetic disease 128 15
C0019562 Von Hippel-Lindau Syndrome disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity; disease of cellular proliferation 170 29
C1847835 VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding) disease Skin and Connective Tissue Diseases Disease or Syndrome 302 92
C0042900 Vitiligo disease Skin and Connective Tissue Diseases Disease or Syndrome disease of anatomical entity Abnormality of the integument 302 92
C0042870 Vitamin D Deficiency disease Nutritional and Metabolic Diseases Disease or Syndrome Abnormality of metabolism/homeostasis 144 27
C0042769 Virus Diseases group Infections Disease or Syndrome disease by infectious agent 1469 42
C0276138 Viral myocarditis disease Infections; Cardiovascular Diseases Disease or Syndrome 128 2
C0025297 Viral meningitis disease Infections; Nervous System Diseases Disease or Syndrome disease of anatomical entity 10 0
C4551858 Vesicoureteral Reflux 1 disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome disease of anatomical entity 46 10
C0042580 Vesico-Ureteral Reflux disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome disease of anatomical entity Abnormality of the genitourinary system 53 6
C0282666 Very Low Birth Weight phenotype Sign or Symptom 42 2
C0085612 Ventricular arrhythmia disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome Abnormality of the cardiovascular system 163 34
C1861172 Venous Thromboembolism phenotype Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 270 106
C0151436 Vasculitis, Leukocytoclastic, Cutaneous disease Immune System Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 18 0
C0042384 Vasculitis disease Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 248 24
C1402315 Vascular lesions disease Disease or Syndrome 111 9
C2004435 Vascular insufficiency of intestine disease Digestive System Diseases; Cardiovascular Diseases Disease or Syndrome 65 0
C0042373 Vascular Diseases group Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 660 40
C3805043 Vascular cognitive impairment disease Disease or Syndrome 42 1
C0042345 Varicosity disease Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 148 20
C0042344 Varicose Ulcer disease Skin and Connective Tissue Diseases; Cardiovascular Diseases Disease or Syndrome 31 2
C0042133 Uterine Fibroids group Neoplasms Neoplastic Process disease of anatomical entity; disease of cellular proliferation Abnormality of the genitourinary system; Neoplasm 528 52
C1704376 Uterine Corpus Carcinosarcoma disease Neoplastic Process disease of anatomical entity; disease of cellular proliferation 33 0