TEK, TEK receptor tyrosine kinase, 7010

N. diseases: 300; N. variants: 17
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: C0153467
Disease: Malignant tumor of peritoneum
Malignant tumor of peritoneum
disease Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 23 1 0.010 None 1.000 1 2019 2019
Epilepsy, Benign Psychomotor, Childhood
disease Nervous System Diseases Disease or Syndrome 23 0.300 None 1.000 1 2007 2007
CUI: C1533041
Disease: Primary congenital glaucoma
Primary congenital glaucoma
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases Disease or Syndrome 24 25 0.160 None 1.000 6 2016 2020
CUI: C3178801
Disease: Stroke, Lacunar
Stroke, Lacunar
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 24 11 0.010 None 1.000 1 2010 2010
CUI: C0038505
Disease: Sturge-Weber Syndrome
Sturge-Weber Syndrome
disease Neoplasms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 25 2 0.010 None 1.000 1 2007 2007
CUI: C0026633
Disease: Mouth Abnormalities
Mouth Abnormalities
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases Congenital Abnormality 26 0.100 None 0
CUI: C0393682
Disease: Epilepsy, Lateral Temporal
Epilepsy, Lateral Temporal
disease Nervous System Diseases Disease or Syndrome 29 1 0.300 None 1.000 1 2007 2007
CUI: C0600452
Disease: Hepatopulmonary Syndrome
Hepatopulmonary Syndrome
disease Digestive System Diseases; Respiratory Tract Diseases Disease or Syndrome 29 1 0.010 None 1.000 1 2018 2018
CUI: C0041316
Disease: Lymph Node Tuberculosis
Lymph Node Tuberculosis
disease Infections Disease or Syndrome 33 1 0.010 None 1.000 1 2018 2018
CUI: C0018920
Disease: Hemangioma, Cavernous
Hemangioma, Cavernous
disease Neoplasms; Hemic and Lymphatic Diseases; Cardiovascular Diseases Neoplastic Process 36 4 0.100 None 0
CUI: C0265950
Disease: Venous malformation
Venous malformation
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 38 3 0.500 strong 1.000 24 1 1996 2019
CUI: C0009766
Disease: Allergic Conjunctivitis
Allergic Conjunctivitis
disease Eye Diseases; Immune System Diseases Disease or Syndrome 38 2 0.010 None 1.000 1 1 2018 2018
CUI: C0684256
Disease: Bacterial sepsis
Bacterial sepsis
disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 38 0.010 None 1.000 1 2017 2017
CUI: C2937220
Disease: Congenital abnormality of vein
Congenital abnormality of vein
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 39 7 0.500 strong 1.000 24 1 1996 2019
CUI: C0700636
Disease: Focal nodular hyperplasia of liver
Focal nodular hyperplasia of liver
disease Digestive System Diseases Disease or Syndrome 39 0.010 None 1.000 1 2003 2003
CUI: C0151529
Disease: Prolonged bleeding time
Prolonged bleeding time
phenotype Finding 39 3 0.100 None 0
CUI: C0340803
Disease: Capillary malformation (disorder)
Capillary malformation (disorder)
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 40 13 0.010 None 1.000 1 2005 2005
CUI: C0041974
Disease: Urethral Stenosis
Urethral Stenosis
phenotype Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 41 1 0.010 None 1.000 1 2017 2017
Gastro-enteropancreatic neuroendocrine tumor
disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 41 4 0.010 None 1.000 1 2010 2010
CUI: C1961121
Disease: Congenital vascular anomaly
Congenital vascular anomaly
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 42 1 0.020 None 1.000 2 2011 2015
CUI: C0042961
Disease: Intestinal Volvulus
Intestinal Volvulus
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 42 2 0.100 None 0
CUI: C0235752
Disease: Port-Wine Stain
Port-Wine Stain
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Congenital Abnormality 46 10 0.100 None 0
CUI: C0344530
Disease: Congenital keratoglobus
Congenital keratoglobus
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Congenital Abnormality 46 9 0.100 None 0
CUI: C0158570
Disease: Vascular anomaly
Vascular anomaly
phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Anatomical Abnormality 47 5 0.050 None 1.000 5 3 2011 2019
CUI: C2215101
Disease: Acute cerebral ischemia
Acute cerebral ischemia
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 47 2 0.010 None 1.000 1 1 2016 2016