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: C0264856
Disease: Giant cell myocarditis
Giant cell myocarditis 		disease Cardiovascular Diseases Disease or Syndrome 2 0.010 None 1.000 1 2009 2009
CUI: C0154754
Disease: Hereditary and idiopathic neuropathy, unspecified
Hereditary and idiopathic neuropathy, unspecified 		disease Nervous System Diseases Disease or Syndrome 3 6 0.100 None 1.000 1 2 2017 2017
CUI: C4310713
Disease: MACULAR DYSTROPHY, PATTERNED, 3
MACULAR DYSTROPHY, PATTERNED, 3 		disease Disease or Syndrome 3 1 0.010 None 1.000 1 2016 2016
CUI: C4748608
Disease: NEUROPATHY, CONGENITAL HYPOMYELINATING, 3
NEUROPATHY, CONGENITAL HYPOMYELINATING, 3 		disease Disease or Syndrome 4 13 0.100 None 1.000 1 2 2017 2017
CUI: C4722277
Disease: NEUROPATHY, CONGENITAL HYPOMYELINATING, 2
NEUROPATHY, CONGENITAL HYPOMYELINATING, 2 		disease Disease or Syndrome 5 9 0.100 None 1.000 1 2 2017 2017
CUI: C1536010
Disease: Lymphoma transformation
Lymphoma transformation 		disease Neoplastic Process 6 0.010 None 1.000 1 2003 2003
CUI: C1739388
Disease: Birch pollen allergy
Birch pollen allergy 		disease Disease or Syndrome 6 0.010 None 1.000 1 2009 2009
CUI: C0276721
Disease: Phaeohyphomycosis
Phaeohyphomycosis 		disease Infections Disease or Syndrome 9 0.010 None 1.000 1 2018 2018
CUI: C0276279
Disease: Mink parvovirus infection
Mink parvovirus infection 		disease Infections Disease or Syndrome 10 0.010 None 1.000 1 2019 2019
CUI: C0017672
Disease: Glossalgia
Glossalgia 		phenotype Pathological Conditions, Signs and Symptoms; Stomatognathic Diseases Sign or Symptom 11 0.010 None 1.000 1 2017 2017
CUI: C2242704
Disease: Chronic myeloid leukaemia transformation
Chronic myeloid leukaemia transformation 		disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 11 0.010 None < 0.001 1 2007 2007
CUI: C4546431
Disease: Exacerbation of allergic asthma
Exacerbation of allergic asthma 		disease Disease or Syndrome 11 0.010 None 1.000 1 2020 2020
CUI: C0406486
Disease: Ocular Rosacea
Ocular Rosacea 		disease Skin and Connective Tissue Diseases Disease or Syndrome 12 0.010 None 1.000 1 2017 2017
CUI: C0474368
Disease: Labor Pain
Labor Pain 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 12 1 0.010 None 1.000 1 2019 2019
CUI: C0338715
Disease: Drug-induced depressive state
Drug-induced depressive state 		disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 13 0.300 None 1.000 1 2011 2011
CUI: C1306571
Disease: Hepatic Insufficiency
Hepatic Insufficiency 		phenotype Digestive System Diseases Pathologic Function 13 0.300 None 1.000 1 2018 2018
CUI: C2721566
Disease: Meniscal degeneration
Meniscal degeneration 		disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 13 0.010 None 1.000 1 2008 2008
CUI: C3469526
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP F
FANCONI ANEMIA, COMPLEMENTATION GROUP F 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 13 6 0.010 None 1.000 1 2012 2012
CUI: C0400807
Disease: Stress ulcer of stomach
Stress ulcer of stomach 		disease Digestive System Diseases Disease or Syndrome 14 0.010 None < 0.001 1 2019 2019
CUI: C2741638
Disease: Stress ulcer
Stress ulcer 		disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 14 0.010 None < 0.001 1 2019 2019
CUI: C1864040
Disease: Cerebral Cavernous Malformations 3
Cerebral Cavernous Malformations 3 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Stomatognathic Diseases; Behavior and Behavior Mechanisms Disease or Syndrome 15 9 0.010 None 1.000 1 2009 2009
CUI: C2363866
Disease: Traumatic occlusion
Traumatic occlusion 		disease Disease or Syndrome 15 0.010 None 1.000 1 2017 2017
CUI: C3873363
Disease: Acute pulmonary thromboembolism
Acute pulmonary thromboembolism 		disease Respiratory Tract Diseases; Cardiovascular Diseases Disease or Syndrome 15 0.010 None 1.000 1 2019 2019
CUI: C0220724
Disease: CONSTRICTING BANDS, CONGENITAL
CONSTRICTING BANDS, CONGENITAL 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 16 1 0.010 None < 0.001 1 2012 2012
CUI: C2242710
Disease: Intra-Abdominal Hypertension
Intra-Abdominal Hypertension 		disease Musculoskeletal Diseases; Cardiovascular Diseases Disease or Syndrome 17 0.010 None 1.000 1 2016 2016