MOK, MOK protein kinase, 5891

N. diseases: 251; N. variants: 11
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: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
phenotype Neoplastic Process 6626 169 0.070 None 1.000 7 1 2011 2018
Malignant neoplasm of colon and/or rectum
disease Neoplastic Process 3669 502 0.020 None 1.000 2 1 2011 2016
Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site
disease Disease or Syndrome 467 14 0.010 None 1.000 1 2017 2017
CUI: C0423719
Disease: Central post-stroke pain
Central post-stroke pain
phenotype Sign or Symptom 9 0.010 None 1.000 1 2018 2018
Red cell distribution width determination
phenotype Laboratory Procedure 593 988 0.100 None 1.000 1 1 2019 2019
CUI: C0549523
Disease: Oropharynx (excludes nasopharynx)
Oropharynx (excludes nasopharynx)
disease Disease or Syndrome 94 5 0.010 None 1.000 1 2002 2002
CUI: C0687131
Disease: Psychoticism
Psychoticism
disease Mental or Behavioral Dysfunction 11 2 0.010 None 1.000 1 1 2012 2012
CUI: C0699753
Disease: Cancer Relapse
Cancer Relapse
disease Neoplastic Process 48 0.010 None 1.000 1 2018 2018
CUI: C0741923
Disease: cardiac event
cardiac event
phenotype Disease or Syndrome 82 18 0.010 None 1.000 1 2008 2008
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction
phenotype Disease or Syndrome 716 25 0.010 None 1.000 1 2008 2008
Finding of Mean Corpuscular Hemoglobin
phenotype Finding 653 1206 0.100 None 1.000 1 1 2019 2019
CUI: C1262048
Disease: Glial scar
Glial scar
phenotype Acquired Abnormality 51 0.010 None 1.000 1 2014 2014
RDW - Red blood cell distribution width result
phenotype Laboratory or Test Result 593 988 0.100 None 1.000 1 1 2019 2019
CUI: C1305855
Disease: Body mass index
Body mass index
phenotype Clinical Attribute 1014 2689 0.100 None 1.000 1 1 2019 2019
CUI: C1969372
Disease: Tubulointerstitial fibrosis
Tubulointerstitial fibrosis
phenotype Disease or Syndrome 328 0.010 None 1.000 1 2018 2018
CUI: C2363774
Disease: Neutrophilic asthma
Neutrophilic asthma
disease Disease or Syndrome 40 2 0.010 None 1.000 1 1 2018 2018
CUI: C2363819
Disease: Paucigranulocytic asthma
Paucigranulocytic asthma
disease Disease or Syndrome 10 0.010 None 1.000 1 2017 2017
CUI: C2894027
Disease: Post traumatic osteoarthritis
Post traumatic osteoarthritis
disease Disease or Syndrome 22 0.010 None 1.000 1 2018 2018
CUI: C2945695
Disease: Limb ischemia
Limb ischemia
disease Disease or Syndrome 171 3 0.010 None 1.000 1 2019 2019
CUI: C3160909
Disease: Autoimmune arthritis
Autoimmune arthritis
disease Disease or Syndrome 113 0.010 None 1.000 1 2016 2016
Obesity-Associated Insulin Resistance
disease Disease or Syndrome 36 0.010 None 1.000 1 2014 2014
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease
disease Disease or Syndrome 741 81 0.010 None < 0.001 1 2018 2018
CUI: C4721773
Disease: Postoperative cognitive dysfunction
Postoperative cognitive dysfunction
phenotype Mental or Behavioral Dysfunction 93 0.010 None 1.000 1 2017 2017
CUI: C4728046
Disease: Diabetic wound
Diabetic wound
disease Disease or Syndrome 72 0.010 None 1.000 1 2017 2017
CUI: C4732837
Disease: Leptomeningeal enhancement
Leptomeningeal enhancement
phenotype Anatomical Abnormality 6 1 0.010 None 1.000 1 2020 2020