STK4, serine/threonine kinase 4, 6789

N. diseases: 58; N. variants: 5
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.
T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AUTOIMMUNITY, AND CARDIAC MALFORMATIONS
phenotype Finding 1 0.300 strong 1.000 2 2012 2014
T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AND AUTOIMMUNITY WITH OR WITHOUT CARDIAC MALFORMATIONS
disease Disease or Syndrome 8 1 0.730 limited 1.000 5 1 2012 2018
CUI: C4289709
Disease: DOCK8 Deficiency
DOCK8 Deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 18 0.010 None 1.000 1 2015 2015
CUI: C1844384
Disease: Recurrent fungal infections
Recurrent fungal infections
phenotype Finding 20 2 0.100 None 0
CUI: C1837066
Disease: Recurrent viral infection
Recurrent viral infection
phenotype Infections Finding 32 0.100 None 0
CUI: C3887645
Disease: Job Syndrome
Job Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 35 12 0.010 None 1.000 1 2015 2015
CUI: C0236773
Disease: Depressed bipolar I disorder
Depressed bipolar I disorder
disease Mental Disorders Mental or Behavioral Dysfunction 37 59 0.100 None 1.000 1 1 2019 2019
CUI: C3665596
Disease: Warts
Warts
disease Infections; Skin and Connective Tissue Diseases Neoplastic Process 39 3 0.100 None 0
CUI: C0043037
Disease: Common wart
Common wart
disease Neoplasms; Infections; Skin and Connective Tissue Diseases Disease or Syndrome 48 0.100 None 0
CUI: C1844383
Disease: Recurrent bacterial infection
Recurrent bacterial infection
phenotype Infections Finding 69 0.100 None 0
CUI: C1840311
Disease: Laryngeal cleft
Laryngeal cleft
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 72 4 0.010 None 1.000 1 2017 2017
CUI: C0242172
Disease: Pelvic Inflammatory Disease
Pelvic Inflammatory Disease
group Female Urogenital Diseases and Pregnancy Complications; Infections Disease or Syndrome 74 3 0.010 None 1.000 1 2018 2018
CUI: C0024713
Disease: Manic Disorder
Manic Disorder
disease Mental Disorders Mental or Behavioral Dysfunction 76 0.300 None 1.000 1 2019 2019
CUI: C2945759
Disease: aggressive cancer
aggressive cancer
phenotype Neoplastic Process 83 5 0.010 None 1.000 1 2017 2017
CUI: C0494261
Disease: Combined immunodeficiency
Combined immunodeficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases Disease or Syndrome 86 11 0.310 strong 1.000 2 2014 2015
CUI: C0005587
Disease: Depression, Bipolar
Depression, Bipolar
disease Mental Disorders Mental or Behavioral Dysfunction 116 2 0.300 None 1.000 1 2019 2019
CUI: C1850900
Disease: Familial primary gastric lymphoma
Familial primary gastric lymphoma
disease Digestive System Diseases; Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 121 2 0.010 None 1.000 1 2016 2016
CUI: C0340643
Disease: Dissection of aorta
Dissection of aorta
disease Cardiovascular Diseases Disease or Syndrome 152 16 0.010 None 1.000 1 2018 2018
CUI: C0338831
Disease: Manic
Manic
disease Mental Disorders Mental or Behavioral Dysfunction 166 8 0.300 None 1.000 1 2019 2019
Pancreatic intraepithelial neoplasia
disease Neoplasms Neoplastic Process 186 11 0.010 None 1.000 1 2014 2014
CUI: C0024312
Disease: Lymphopenia
Lymphopenia
disease Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 239 16 0.120 None 1.000 2 2016 2018
Mucosa-Associated Lymphoid Tissue Lymphoma
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 264 13 0.010 None 1.000 1 2016 2016
CUI: C1292778
Disease: Chronic myeloproliferative disorder
Chronic myeloproliferative disorder
disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 366 47 0.010 None 1.000 1 2019 2019
CUI: C0149678
Disease: Epstein-Barr Virus Infections
Epstein-Barr Virus Infections
group Infections Disease or Syndrome 384 72 0.010 None 1.000 1 2018 2018
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 384 96 0.100 None 0