CASP3, caspase 3, 836

N. diseases: 819; N. variants: 26
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: C0242852
Disease: Proliferative vitreoretinopathy
Proliferative vitreoretinopathy
disease Eye Diseases Disease or Syndrome 142 14 0.010 None 1.000 1 2017 2017
CUI: C0243010
Disease: Viral Encephalitis
Viral Encephalitis
group Infections; Nervous System Diseases Disease or Syndrome 35 0.010 None 1.000 1 2019 2019
CUI: C0243038
Disease: Carcinoma, Lewis Lung
Carcinoma, Lewis Lung
disease Neoplasms Neoplastic Process; Experimental Model of Disease 188 0.010 None 1.000 1 2018 2018
CUI: C0262401
Disease: Carcinoma of ampulla of Vater
Carcinoma of ampulla of Vater
disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 37 4 0.010 None 1.000 1 2013 2013
CUI: C0262404
Disease: Cerebellar degeneration
Cerebellar degeneration
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 60 0.010 None 1.000 1 1998 1998
CUI: C0262929
Disease: Myxoma of the Endocardium
Myxoma of the Endocardium
disease Neoplasms Neoplastic Process 28 0.010 None 1.000 1 2005 2005
CUI: C0263361
Disease: Psoriasis vulgaris
Psoriasis vulgaris
disease Skin and Connective Tissue Diseases Disease or Syndrome 255 80 0.010 None 1.000 1 2017 2017
CUI: C0264714
Disease: Acute heart failure
Acute heart failure
disease Cardiovascular Diseases Disease or Syndrome 89 0.010 None 1.000 1 2018 2018
CUI: C0265325
Disease: Turcot syndrome (disorder)
Turcot syndrome (disorder)
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nervous System Diseases Disease or Syndrome 77 75 0.010 None 1.000 1 2019 2019
CUI: C0302142
Disease: Deformity
Deformity
group Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Anatomical Abnormality 350 26 0.010 None 1.000 1 2019 2019
CUI: C0302809
Disease: Fulminant hepatitis
Fulminant hepatitis
disease Digestive System Diseases Disease or Syndrome 57 1 0.010 None 1.000 1 2019 2019
CUI: C0332853
Disease: Anastomosis
Anastomosis
disease Acquired Abnormality 155 2 0.010 None 1.000 1 2018 2018
Histiocytic Necrotizing Lymphadenitis
disease Hemic and Lymphatic Diseases Disease or Syndrome 14 0.010 None 1.000 1 2004 2004
CUI: C0398650
Disease: Immune thrombocytopenic purpura
Immune thrombocytopenic purpura
disease Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 338 35 0.010 None 1.000 1 2019 2019
CUI: C0403823
Disease: Asthenozoospermia
Asthenozoospermia
disease Male Urogenital Diseases Disease or Syndrome 164 17 0.010 None 1.000 1 2014 2014
CUI: C0410207
Disease: Tubular Aggregate Myopathy
Tubular Aggregate Myopathy
disease Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 67 5 0.010 None 1.000 1 2019 2019
CUI: C0431406
Disease: Asymmetric crying face association
Asymmetric crying face association
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Stomatognathic Diseases Disease or Syndrome 25 2 0.010 None 1.000 1 2017 2017
Secondary malignant neoplasm of liver
disease Digestive System Diseases; Neoplasms Neoplastic Process 951 34 0.010 None 1.000 1 2007 2007
CUI: C0521158
Disease: Recurrent tumor
Recurrent tumor
phenotype Neoplastic Process 735 33 0.010 None 1.000 1 2015 2015
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
disease Digestive System Diseases; Infections Disease or Syndrome 430 80 0.010 None 1.000 1 2008 2008
CUI: C0549523
Disease: Oropharynx (excludes nasopharynx)
Oropharynx (excludes nasopharynx)
disease Disease or Syndrome 94 5 0.010 None 1.000 1 2019 2019
CUI: C0553580
Disease: Ewings sarcoma
Ewings sarcoma
disease Neoplasms Neoplastic Process 517 25 0.010 None 1.000 1 2018 2018
CUI: C0558353
Disease: Tongue Carcinoma
Tongue Carcinoma
disease Neoplasms; Stomatognathic Diseases Neoplastic Process 157 2 0.010 None 1.000 1 2009 2009
CUI: C0575064
Disease: Skeletal muscle tender
Skeletal muscle tender
phenotype Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases Sign or Symptom 4 0.010 None 1.000 1 2019 2019
CUI: C0584960
Disease: Factor V Leiden mutation
Factor V Leiden mutation
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 86 46 0.010 None 1.000 1 2015 2015