MAPK14, mitogen-activated protein kinase 14, 1432

N. diseases: 626; N. variants: 7
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: C0151565
Disease: Hemorrhagic colitis
Hemorrhagic colitis 		disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 18 0.010 None 1.000 1 2019 2019
CUI: C0268251
Disease: Gaucher Disease, Type 3 (disorder)
Gaucher Disease, Type 3 (disorder) 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 18 26 0.010 None 1.000 1 2015 2015
CUI: C1455780
Disease: Aortic valve sclerosis
Aortic valve sclerosis 		disease Nutritional and Metabolic Diseases; Cardiovascular Diseases Disease or Syndrome 18 0.010 None 1.000 1 2018 2018
CUI: C0015974
Disease: Periodic fever
Periodic fever 		disease Disease or Syndrome 19 5 0.010 None 1.000 1 2011 2011
CUI: C0428796
Disease: Senile sclerosis of aortic cusp
Senile sclerosis of aortic cusp 		disease Disease or Syndrome 19 0.010 None 1.000 1 2018 2018
CUI: C0796135
Disease: Renpenning syndrome 1
Renpenning syndrome 1 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 19 5 0.010 None 1.000 1 2017 2017
CUI: C0025306
Disease: Meningococcemia
Meningococcemia 		disease Infections Disease or Syndrome 20 0.010 None < 0.001 1 2011 2011
CUI: C1262117
Disease: Fungal keratitis
Fungal keratitis 		disease Pathological Conditions, Signs and Symptoms; Infections; Eye Diseases Disease or Syndrome 21 3 0.010 None 1.000 1 2017 2017
CUI: C1319466
Disease: Barber Say syndrome
Barber Say syndrome 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Stomatognathic Diseases Disease or Syndrome 21 4 0.010 None 1.000 1 2012 2012
CUI: C0233477
Disease: Dysphoric mood
Dysphoric mood 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 22 6 0.300 None 1.000 1 2007 2007
CUI: C3468041
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP C
FANCONI ANEMIA, COMPLEMENTATION GROUP C 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 22 73 0.010 None 1.000 1 2017 2017
CUI: C0278147
Disease: Radicular pain
Radicular pain 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 23 5 0.010 None 1.000 1 2019 2019
CUI: C2348101
Disease: Destructive Arthritis
Destructive Arthritis 		disease Musculoskeletal Diseases Disease or Syndrome 23 0.010 None 1.000 1 2005 2005
CUI: C0036396
Disease: Sciatica
Sciatica 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 24 4 0.010 None 1.000 1 2018 2018
CUI: C1834523
Disease: ARTHROGRYPOSIS, DISTAL, TYPE 2B
ARTHROGRYPOSIS, DISTAL, TYPE 2B 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 25 6 0.010 None 1.000 1 2017 2017
CUI: C1849508
Disease: EPILEPSY, PYRIDOXINE-DEPENDENT
EPILEPSY, PYRIDOXINE-DEPENDENT 		disease Nervous System Diseases Disease or Syndrome 25 26 0.010 None 1.000 1 2009 2009
CUI: C0036330
Disease: Schistosomiasis mansoni
Schistosomiasis mansoni 		disease Infections Disease or Syndrome 27 0.010 None 1.000 1 2003 2003
CUI: C0270726
Disease: Alexander Disease
Alexander Disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 27 99 0.010 None 1.000 1 2008 2008
CUI: C0007192
Disease: Cardiomyopathy, Alcoholic
Cardiomyopathy, Alcoholic 		disease Chemically-Induced Disorders; Cardiovascular Diseases Disease or Syndrome 30 0.010 None 1.000 1 2018 2018
CUI: C0019087
Disease: Hemorrhagic Disorders
Hemorrhagic Disorders 		group Hemic and Lymphatic Diseases Disease or Syndrome 30 3 0.010 None 1.000 1 2006 2006
CUI: C0409818
Disease: Chronic Infantile Neurological, Cutaneous, and Articular Syndrome
Chronic Infantile Neurological, Cutaneous, and Articular Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 30 22 0.010 None 1.000 1 2005 2005
CUI: C1395512
Disease: Placental dysfunction
Placental dysfunction 		disease Disease or Syndrome 31 0.010 None 1.000 1 2010 2010
CUI: C1290807
Disease: Diarrheal disorder
Diarrheal disorder 		disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 32 0.010 None 1.000 1 2019 2019
CUI: C1861303
Disease: SYNOVITIS, GRANULOMATOUS, WITH UVEITIS AND CRANIAL NEUROPATHIES (disorder)
SYNOVITIS, GRANULOMATOUS, WITH UVEITIS AND CRANIAL NEUROPATHIES (disorder) 		disease Eye Diseases; Musculoskeletal Diseases Disease or Syndrome 33 22 0.010 None 1.000 1 2015 2015
CUI: C4316909
Disease: Marijuana Use
Marijuana Use 		disease Mental Disorders; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 33 0.010 None 1.000 1 2013 2013