MBP, myelin basic protein, 4155

N. diseases: 184; 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: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
disease Immune System Diseases; Nervous System Diseases Disease or Syndrome 1800 1022 0.100 None 0.939 163 1990 2020
CUI: C0011303
Disease: Demyelinating Diseases
Demyelinating Diseases
group Nervous System Diseases Disease or Syndrome 156 5 0.580 None 1.000 10 1985 2017
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
disease Mental Disorders Mental or Behavioral Dysfunction 2872 2897 0.580 None 0.750 10 2006 2019
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
group Immune System Diseases Disease or Syndrome 1758 428 0.090 None 1.000 9 1997 2014
CUI: C0027651
Disease: Neoplasms
Neoplasms
group Neoplasms Neoplastic Process 10161 1644 0.060 None 1.000 6 1996 2017
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 1883 1172 0.050 None 0.800 5 1995 2019
CUI: C0026269
Disease: Mitral Valve Stenosis
Mitral Valve Stenosis
disease Cardiovascular Diseases Disease or Syndrome 170 7 0.050 None 1.000 5 1993 2017
CUI: C3495421
Disease: Chromosome 18q syndrome
Chromosome 18q syndrome
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 4 0.040 None 1.000 4 1992 2003
CUI: C0809935
Disease: Chromosome 18, trisomy 18q
Chromosome 18, trisomy 18q
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 5 0.040 None 1.000 4 1992 2003
Deletion of long arm of chromosome 18
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 6 0.040 None 1.000 4 1992 2003
CUI: C0524851
Disease: Neurodegenerative Disorders
Neurodegenerative Disorders
group Nervous System Diseases Disease or Syndrome 1515 85 0.040 None 1.000 4 2012 2018
CUI: C0221505
Disease: Lesion of brain
Lesion of brain
group Disease or Syndrome 188 9 0.040 None 1.000 4 1993 1997
CUI: C0027873
Disease: Neuromyelitis Optica
Neuromyelitis Optica
disease Eye Diseases; Immune System Diseases; Nervous System Diseases Disease or Syndrome 171 45 0.330 None 1.000 4 2008 2018
CUI: C0555198
Disease: Malignant Glioma
Malignant Glioma
disease Neoplasms Neoplastic Process 724 22 0.030 None 1.000 3 1997 2000
CUI: C0740391
Disease: Middle Cerebral Artery Occlusion
Middle Cerebral Artery Occlusion
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Acquired Abnormality 626 0.030 None 1.000 3 2017 2019
Well Differentiated Oligodendroglioma
disease Neoplasms Neoplastic Process 270 22 0.030 None 1.000 3 1993 2002
Experimental Autoimmune Encephalomyelitis
disease Immune System Diseases; Nervous System Diseases Experimental Model of Disease 97 0.300 None 1.000 3 2000 2013
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
disease Nervous System Diseases; Mental Disorders Disease or Syndrome 3397 1843 0.030 None 1.000 3 2009 2014
Multiple Sclerosis, Relapsing-Remitting
disease Immune System Diseases; Nervous System Diseases Disease or Syndrome 206 7 0.030 None 1.000 3 1997 2016
CUI: C0028945
Disease: oligodendroglioma
oligodendroglioma
disease Neoplasms Neoplastic Process 282 21 0.030 None 1.000 3 1993 2002
CUI: C0027809
Disease: Neurilemmoma
Neurilemmoma
disease Neoplasms Neoplastic Process 193 11 0.030 None 1.000 3 1999 2019
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
disease Neoplasms; Immune System Diseases; Nervous System Diseases Disease or Syndrome 336 93 0.030 None 1.000 3 1989 1994
CUI: C0023529
Disease: Leukomalacia, Periventricular
Leukomalacia, Periventricular
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 62 10 0.210 None 1.000 2 2013 2018
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 83 46 0.020 None 1.000 2 2005 2018
CUI: C0205711
Disease: Pelizaeus-Merzbacher Disease
Pelizaeus-Merzbacher Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 30 30 0.020 None 1.000 2 1993 1999