MECP2, methyl-CpG binding protein 2, 4204

N. diseases: 664; N. variants: 387
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: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
disease Neoplasms; Respiratory Tract Diseases Neoplastic Process 4173 1142 0.010 None 1.000 1 2016 2016
CUI: C0266463
Disease: Lissencephaly
Lissencephaly
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality 71 9 0.010 None 1.000 1 2019 2019
CUI: C0729531
Disease: Viral respiratory infection
Viral respiratory infection
group Infections; Respiratory Tract Diseases Disease or Syndrome 33 0.010 None 1.000 1 2017 2017
CUI: C0281902
Disease: maladjustment
maladjustment
phenotype Mental or Behavioral Dysfunction 13 0.010 None 1.000 1 2005 2005
CUI: C0024776
Disease: Maple Syrup Urine Disease
Maple Syrup Urine Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 24 134 0.010 None 1.000 1 2019 2019
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 1881 283 0.010 None 1.000 1 2019 2019
CUI: C0024534
Disease: Malaria, Cerebral
Malaria, Cerebral
disease Infections; Nervous System Diseases Disease or Syndrome 148 34 0.010 None 1.000 1 2017 2017
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis
disease Respiratory Tract Diseases Disease or Syndrome 803 63 0.010 None 1.000 1 2014 2014
CUI: C0340486
Disease: Induced ventricular tachycardia
Induced ventricular tachycardia
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 4 0.010 None 1.000 1 2011 2011
CUI: C0024299
Disease: Lymphoma
Lymphoma
group Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 1548 91 0.010 None 1.000 1 2017 2017
CUI: C2747816
Disease: Complicated malaria
Complicated malaria
disease Infections Disease or Syndrome 166 38 0.010 None 1.000 1 2015 2015
CUI: C0026210
Disease: Mirror Writing
Mirror Writing
phenotype Sign or Symptom 1 0.010 None 1.000 1 2007 2007
CUI: C0265535
Disease: Trigonocephaly
Trigonocephaly
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 52 7 0.010 None 1.000 1 2002 2002
CUI: C0242723
Disease: Parasitemia
Parasitemia
disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 140 3 0.010 None 1.000 1 2009 2009
CUI: C0242852
Disease: Proliferative vitreoretinopathy
Proliferative vitreoretinopathy
disease Eye Diseases Disease or Syndrome 142 14 0.010 None 1.000 1 2015 2015
CUI: C0026847
Disease: Spinal Muscular Atrophy
Spinal Muscular Atrophy
disease Nervous System Diseases Disease or Syndrome 320 33 0.010 None 1.000 1 2007 2007
Mental Retardation, X-Linked, Syndromic, Christianson Type
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Disease or Syndrome 6 13 0.010 None 1.000 1 2014 2014
CUI: C0206696
Disease: Carcinoma, Signet Ring Cell
Carcinoma, Signet Ring Cell
disease Neoplasms Neoplastic Process 70 6 0.010 None 1.000 1 2003 2003
CUI: C0264716
Disease: Chronic heart failure
Chronic heart failure
disease Cardiovascular Diseases Disease or Syndrome 223 11 0.010 None 1.000 1 2015 2015
CUI: C0265101
Disease: Carotid artery occlusion
Carotid artery occlusion
phenotype Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 74 1 0.010 None 1.000 1 2017 2017
CUI: C0265372
Disease: Fetal hydantoin syndrome
Fetal hydantoin syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 11 1 0.010 None 1.000 1 2012 2012
CUI: C0026499
Disease: Monosomy
Monosomy
group Pathological Conditions, Signs and Symptoms Congenital Abnormality 214 11 0.010 None 1.000 1 2015 2015
CUI: C0024143
Disease: Lupus Nephritis
Lupus Nephritis
disease Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases; Male Urogenital Diseases; Immune System Diseases Disease or Syndrome 503 64 0.010 None 1.000 1 2012 2012
Lipoid congenital adrenal hyperplasia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 5 34 0.010 None 1.000 1 2007 2007
Lupus Erythematosus, Subacute Cutaneous
disease Skin and Connective Tissue Diseases Disease or Syndrome 39 1 0.010 None 1.000 1 2008 2008