MAPKAPK3, MAPK activated protein kinase 3, 7867

N. diseases: 19; N. variants: 8
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: C4310713
Disease: MACULAR DYSTROPHY, PATTERNED, 3
MACULAR DYSTROPHY, PATTERNED, 3
disease Disease or Syndrome 3 1 0.510 None 1.000 2 1 2016 2016
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
disease Neoplasms Neoplastic Process 3197 186 0.300 None 0 1
Macular Dystrophy, Butterfly-Shaped Pigmentary, 2
disease Eye Diseases Disease or Syndrome 3 4 0.300 None 0
Patterned dystrophy of retinal pigment epithelium
disease Eye Diseases Disease or Syndrome 3 0.300 None 0
CUI: C0429908
Disease: Susceptibility to tuberculosis
Susceptibility to tuberculosis
phenotype Finding 1 1 0.100 None 0 1
CUI: C0423421
Disease: Atrophic macular change
Atrophic macular change
phenotype Finding 24 1 0.100 None 0
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity
phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Finding 147 10 0.100 None 0
MALARIA, SUSCEPTIBILITY TO (finding)
disease Finding 5 23 0.100 None 0 1
CUI: C3280647
Disease: BACTEREMIA, SUSCEPTIBILITY TO, 2
BACTEREMIA, SUSCEPTIBILITY TO, 2
phenotype Finding 1 1 0.100 None 0 1
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 194 33 0.100 None 0
CUI: C1288283
Disease: Atrophoderma maculatum
Atrophoderma maculatum
disease Skin and Connective Tissue Diseases Disease or Syndrome 39 2 0.100 None 0
ANOPHTHALMIA AND PULMONARY HYPOPLASIA
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Respiratory Tract Diseases Disease or Syndrome 1410 80 0.010 None 1.000 1 2016 2016
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
disease Digestive System Diseases; Neoplasms Neoplastic Process 5473 1962 0.010 None 1.000 1 2019 2019
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
disease Digestive System Diseases; Infections Disease or Syndrome 430 80 0.010 None 1.000 1 2009 2009
CUI: C0221232
Disease: Welts
Welts
phenotype Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Immune System Diseases Sign or Symptom 53 0.010 None 1.000 1 2011 2011
CUI: C0042109
Disease: Urticaria
Urticaria
disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 168 11 0.010 None 1.000 1 2011 2011
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases
group Eye Diseases Disease or Syndrome 714 56 0.010 None 1.000 1 2016 2016
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
disease Digestive System Diseases; Infections Disease or Syndrome 1768 347 0.010 None 1.000 1 2 2009 2009
Malignant neoplasm of colon and/or rectum
disease Neoplastic Process 3669 502 0.010 None 1.000 1 2019 2019