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: C0341037
Disease: Lateral developmental cyst of jaw
Lateral developmental cyst of jaw
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Musculoskeletal Diseases; Respiratory Tract Diseases; Stomatognathic Diseases Congenital Abnormality 1 0.010 None 1.000 1 2017 2017
CUI: C0231813
Disease: Meningitic respiration
Meningitic respiration
phenotype Sign or Symptom 2 0.010 None 1.000 1 2017 2017
CUI: C4552167
Disease: Reoviral infection
Reoviral infection
disease Disease or Syndrome 2 0.010 None 1.000 1 2018 2018
CUI: C0393971
Disease: Spinal cord stroke
Spinal cord stroke
disease Nervous System Diseases; Cardiovascular Diseases; Wounds and Injuries Disease or Syndrome 3 0.020 None 1.000 2 2000 2004
CUI: C0014476
Disease: Eperythrozoonosis
Eperythrozoonosis
disease Infections Disease or Syndrome 3 0.300 None 1.000 1 2010 2010
CUI: C0085412
Disease: Encephalitozoonosis
Encephalitozoonosis
disease Infections Disease or Syndrome 3 0.010 None 1.000 1 2006 2006
CUI: C0852862
Disease: Perinatal brain damage
Perinatal brain damage
disease Disease or Syndrome 3 0.010 None 1.000 1 2001 2001
CUI: C3266060
Disease: Botryoid odontogenic cyst
Botryoid odontogenic cyst
disease Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases Disease or Syndrome 3 0.010 None 1.000 1 2017 2017
CUI: C0240419
Disease: Muscle tenderness
Muscle tenderness
phenotype Musculoskeletal Diseases Sign or Symptom 4 0.010 None 1.000 1 2019 2019
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: C0041312
Disease: Tuberculosis, Gastrointestinal
Tuberculosis, Gastrointestinal
disease Digestive System Diseases; Infections Disease or Syndrome 6 0.010 None 1.000 1 2016 2016
CUI: C1862112
Disease: BRACHYDACTYLY, TYPE B1
BRACHYDACTYLY, TYPE B1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 6 8 0.010 None 1.000 1 2018 2018
CUI: C0042995
Disease: Vulvar Neoplasms
Vulvar Neoplasms
group Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 7 0.010 None 1.000 1 2007 2007
CUI: C1112338
Disease: Apoptotic DNA damage
Apoptotic DNA damage
disease Disease or Syndrome 7 0.010 None 1.000 1 2018 2018
CUI: C0238097
Disease: Cytomegalovirus encephalitis
Cytomegalovirus encephalitis
disease Infections; Nervous System Diseases Disease or Syndrome 8 0.010 None 1.000 1 2017 2017
CUI: C0270192
Disease: Perinatal Subarachnoid Hemorrhage
Perinatal Subarachnoid Hemorrhage
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 8 0.300 None 1.000 1 2014 2014
Subarachnoid Hemorrhage, Spontaneous
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 8 0.300 None 1.000 1 2014 2014
CUI: C0751530
Disease: Subarachnoid Hemorrhage, Aneurysmal
Subarachnoid Hemorrhage, Aneurysmal
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 8 0.300 None 1.000 1 2014 2014
Subarachnoid Hemorrhage, Intracranial
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 8 0.300 None 1.000 1 2014 2014
CUI: C1412014
Disease: Infiltrating duct carcinoma
Infiltrating duct carcinoma
disease Neoplasms Neoplastic Process 8 0.010 None 1.000 1 2006 2006
CUI: C1563730
Disease: Abdominal Cryptorchidism
Abdominal Cryptorchidism
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases Congenital Abnormality 8 0.300 None 1.000 1 2015 2015
CUI: C1563731
Disease: Inguinal Cryptorchidism
Inguinal Cryptorchidism
phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases Finding 8 0.300 None 1.000 1 2015 2015
CUI: C2266788
Disease: Trichilemmal cyst
Trichilemmal cyst
disease Neoplasms Disease or Syndrome 8 2 0.010 None < 0.001 1 2011 2011
Squamous cell carcinoma of buccal mucosa
disease Neoplasms Neoplastic Process 9 0.010 None 1.000 1 2017 2017
CUI: C1334807
Disease: Mucinous carcinoma of breast
Mucinous carcinoma of breast
disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 10 0.010 None 1.000 1 2017 2017