MAPK8, mitogen-activated protein kinase 8, 5599

N. diseases: 520; N. variants: 4
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: C3696954
Disease: Precapillary pulmonary hypertension
Precapillary pulmonary hypertension
disease Respiratory Tract Diseases Disease or Syndrome 1 1 0.010 None 1.000 1 1 2014 2014
CUI: C1262148
Disease: Grip strength decreased
Grip strength decreased
phenotype Sign or Symptom 3 0.010 None 1.000 1 2005 2005
CUI: C1832586
Disease: DERMATITIS HERPETIFORMIS, FAMILIAL
DERMATITIS HERPETIFORMIS, FAMILIAL
disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 3 0.010 None 1.000 1 2017 2017
CUI: C3826634
Disease: Bronchitis in children
Bronchitis in children
disease Disease or Syndrome 4 0.010 None 1.000 1 2017 2017
CUI: C0008272
Disease: Asiderotic anemia
Asiderotic anemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 5 0.010 None 1.000 1 2018 2018
CUI: C0027073
Disease: Myofascial Pain Syndromes
Myofascial Pain Syndromes
disease Musculoskeletal Diseases Disease or Syndrome 5 0.010 None 1.000 1 2019 2019
CUI: C1959589
Disease: Angioma, Cavernous
Angioma, Cavernous
disease Neoplasms; Hemic and Lymphatic Diseases; Cardiovascular Diseases Neoplastic Process 9 0.010 None 1.000 1 2018 2018
CUI: C0796195
Disease: Waisman syndrome
Waisman syndrome
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Disease or Syndrome 10 4 0.010 None 1.000 1 2012 2012
CUI: C0281773
Disease: Acute glaucoma
Acute glaucoma
disease Disease or Syndrome 11 0.010 None 1.000 1 2019 2019
CUI: C0752351
Disease: Embryo Loss
Embryo Loss
phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications Pathologic Function 11 0.010 None 1.000 1 2004 2004
CUI: C0393786
Disease: Trigeminal Neuralgia, Idiopathic
Trigeminal Neuralgia, Idiopathic
disease Nervous System Diseases; Stomatognathic Diseases Disease or Syndrome 12 0.300 None 1.000 1 2016 2016
CUI: C0393787
Disease: Secondary Trigeminal Neuralgia
Secondary Trigeminal Neuralgia
disease Nervous System Diseases; Stomatognathic Diseases Disease or Syndrome 12 0.300 None 1.000 1 2016 2016
Childhood Chronic Myelogenous Leukemia, BCR-ABL1 Positive
disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 12 1 0.010 None 1.000 1 2011 2011
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: C1863844
Disease: Adult-onset citrullinemia type 2
Adult-onset citrullinemia type 2
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 14 15 0.010 None 1.000 1 2015 2015
CUI: C2363866
Disease: Traumatic occlusion
Traumatic occlusion
disease Disease or Syndrome 15 0.010 None 1.000 1 2019 2019
Pneumonia due to Klebsiella pneumoniae
disease Infections; Respiratory Tract Diseases Disease or Syndrome 16 0.010 None 1.000 1 2019 2019
Hyperkeratosis lenticularis perstans
disease Skin and Connective Tissue Diseases Disease or Syndrome 18 11 0.010 None 1.000 1 2000 2000
CUI: C0281658
Disease: Intraocular Lymphoma
Intraocular Lymphoma
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 19 0.010 None 1.000 1 2017 2017
CUI: C0854530
Disease: Infection by human herpesvirus 6
Infection by human herpesvirus 6
disease Infections Disease or Syndrome 19 0.010 None 1.000 1 2012 2012
CUI: C0001193
Disease: Apert syndrome
Apert syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 20 24 0.010 None 1.000 1 2012 2012
CUI: C0342335
Disease: insulin resistance in diabetes
insulin resistance in diabetes
disease Nutritional and Metabolic Diseases Disease or Syndrome 21 1 0.010 None 1.000 1 2003 2003
CUI: C0406557
Disease: Poikiloderma of Kindler
Poikiloderma of Kindler
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Stomatognathic Diseases Disease or Syndrome 21 25 0.010 None 1.000 1 2017 2017
CUI: C0751748
Disease: Nonketotic Hyperglycinemia
Nonketotic Hyperglycinemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 21 182 0.010 None < 0.001 1 2018 2018
CUI: C0221391
Disease: Melanosis coli
Melanosis coli
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 22 5 0.010 None 1.000 1 2019 2019