CDA, cytidine deaminase, 978

N. diseases: 103; N. variants: 9
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: C1167791
Disease: Skin toxicity
Skin toxicity
disease Disease or Syndrome 62 24 0.010 None 1.000 1 2 2017 2017
CUI: C0278488
Disease: Carcinoma breast stage IV
Carcinoma breast stage IV
disease Neoplastic Process 573 14 0.010 None 1.000 1 2018 2018
CUI: C0272051
Disease: Xerocytosis
Xerocytosis
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 20 3 0.010 None 1.000 1 2019 2019
CUI: C1336708
Disease: Testicular Germ Cell Tumor
Testicular Germ Cell Tumor
disease Neoplasms; Male Urogenital Diseases; Endocrine System Diseases Neoplastic Process 208 93 0.010 None 1.000 1 2016 2016
CUI: C0238644
Disease: Anemia, severe
Anemia, severe
disease Hemic and Lymphatic Diseases Disease or Syndrome 65 6 0.010 None < 0.001 1 1 2015 2015
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
group Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 1074 306 0.010 None 1.000 1 2017 2017
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
disease Neoplasms Neoplastic Process 877 43 0.010 None 1.000 1 1 2019 2019
Unilateral Multicystic Dysplastic Kidney
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome; Congenital Abnormality 3 0.010 None 1.000 1 2014 2014
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
phenotype Pathological Conditions, Signs and Symptoms Neoplastic Process 3865 72 0.010 None 1.000 1 2017 2017
CUI: C0175754
Disease: Agenesis of corpus callosum
Agenesis of corpus callosum
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality 615 45 0.010 None 1.000 1 2019 2019
CUI: C0162429
Disease: Malnutrition
Malnutrition
disease Nutritional and Metabolic Diseases Disease or Syndrome 417 29 0.010 None 1.000 1 2019 2019
CUI: C0158266
Disease: Intervertebral Disc Degeneration
Intervertebral Disc Degeneration
disease Musculoskeletal Diseases Disease or Syndrome 342 47 0.010 None 1.000 1 2008 2008
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
disease Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 639 50 0.010 None 1.000 1 2013 2013
Palmar-plantar erythrodysesthesia syndrome
disease Skin and Connective Tissue Diseases; Chemically-Induced Disorders Disease or Syndrome 11 8 0.010 None 1.000 1 2011 2011
CUI: C1260899
Disease: Anemia, Diamond-Blackfan
Anemia, Diamond-Blackfan
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 86 38 0.010 None 1.000 1 2019 2019
CUI: C0038012
Disease: Spondylitis
Spondylitis
disease Infections; Musculoskeletal Diseases Disease or Syndrome 20 0.010 None 1.000 1 2009 2009
CUI: C0282160
Disease: Aplasia Cutis Congenita
Aplasia Cutis Congenita
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Congenital Abnormality 393 14 0.010 None 1.000 1 2019 2019
CUI: C0311276
Disease: Severe malnutrition
Severe malnutrition
disease Disease or Syndrome 13 1 0.010 None 1.000 1 2019 2019
CUI: C0949690
Disease: Spondylarthritis
Spondylarthritis
disease Musculoskeletal Diseases Disease or Syndrome 158 23 0.010 None 1.000 1 2008 2008
CUI: C0879615
Disease: Stromal Neoplasm
Stromal Neoplasm
disease Neoplasms Neoplastic Process 86 1 0.010 None 1.000 1 2015 2015
CUI: C0852711
Disease: Sickle Cell Dactylitis
Sickle Cell Dactylitis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Chemically-Induced Disorders; Hemic and Lymphatic Diseases Disease or Syndrome 8 7 0.010 None 1.000 1 2011 2011
CUI: C0850672
Disease: hereditary anemia
hereditary anemia
disease Disease or Syndrome 4 0.010 None 1.000 1 2019 2019
Infection caused by Helicobacter pylori
disease Infections Disease or Syndrome 337 56 0.010 None 1.000 1 2014 2014
CUI: C0750952
Disease: Biliary Tract Cancer
Biliary Tract Cancer
disease Digestive System Diseases; Neoplasms Neoplastic Process 167 11 0.010 None 1.000 1 2015 2015
Secondary malignant neoplasm of lymph node
disease Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 2825 188 0.010 None < 0.001 1 2017 2017