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: 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: C0393489
Disease: Vacuolar myelopathy
Vacuolar myelopathy 		disease Pathological Conditions, Signs and Symptoms; Infections; Immune System Diseases; Nervous System Diseases Disease or Syndrome 4 0.020 None 1.000 2 1996 2003
CUI: C0007020
Disease: Carbon Monoxide Poisoning
Carbon Monoxide Poisoning 		disease Chemically-Induced Disorders Injury or Poisoning 4 0.200 None 1.000 1 2012 2012
CUI: C0342739
Disease: Trimethylaminuria
Trimethylaminuria 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 4 17 0.010 None 1.000 1 1997 1997
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
CUI: C0432443
Disease: Deletion of long arm of chromosome 18
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: C0030200
Disease: Pain, Intractable
Pain, Intractable 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 6 0.010 None 1.000 1 2017 2017
CUI: C0270780
Disease: Degenerative myelopathy
Degenerative myelopathy 		disease Nervous System Diseases Disease or Syndrome 7 0.010 None 1.000 1 2019 2019
CUI: C0393665
Disease: Multiple Sclerosis, Chronic Progressive
Multiple Sclerosis, Chronic Progressive 		disease Immune System Diseases; Nervous System Diseases Disease or Syndrome 8 0.010 None < 0.001 1 1994 1994
CUI: C1301721
Disease: Neurological morbidity
Neurological morbidity 		disease Disease or Syndrome 8 0.010 None 1.000 1 2018 2018
CUI: C0011304
Disease: Demyelination
Demyelination 		phenotype Nervous System Diseases Pathologic Function 9 0.300 None 1.000 1 1985 1985
CUI: C2350037
Disease: Clinically Isolated Syndrome, CNS Demyelinating
Clinically Isolated Syndrome, CNS Demyelinating 		disease Nervous System Diseases Disease or Syndrome 9 0.300 None 1.000 1 1985 1985
CUI: C0848771
Disease: neurological disability
neurological disability 		phenotype Sign or Symptom 18 6 0.010 None 1.000 1 2018 2018
CUI: C0751689
Disease: Peripheral Nerve Sheath Neoplasm
Peripheral Nerve Sheath Neoplasm 		disease Neoplasms; Nervous System Diseases Neoplastic Process 22 0.010 None 1.000 1 1999 1999
CUI: C0085625
Disease: Hypoalgesia
Hypoalgesia 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders Sign or Symptom 23 7 0.010 None 1.000 1 2018 2018
CUI: C0393814
Disease: Hereditary liability to pressure palsies
Hereditary liability to pressure palsies 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 23 11 0.010 None 1.000 1 1997 1997
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
CUI: C0027813
Disease: Neuritis
Neuritis 		disease Nervous System Diseases Disease or Syndrome 32 0.010 None 1.000 1 1985 1985
CUI: C0742468
Disease: Central nervous system lesion
Central nervous system lesion 		disease Disease or Syndrome 34 1 0.020 None 1.000 2 1998 2017
CUI: C0243010
Disease: Viral Encephalitis
Viral Encephalitis 		group Infections; Nervous System Diseases Disease or Syndrome 35 0.010 None 1.000 1 2005 2005
CUI: C1095979
Disease: Progressive multiple sclerosis
Progressive multiple sclerosis 		disease Disease or Syndrome 37 0.010 None 1.000 1 2017 2017
CUI: C4543807
Disease: Clinical malaria
Clinical malaria 		disease Infections Disease or Syndrome 37 3 0.010 None 1.000 1 1998 1998
CUI: C0276609
Disease: Acute type B viral hepatitis
Acute type B viral hepatitis 		disease Digestive System Diseases; Infections Disease or Syndrome 38 0.010 None 1.000 1 1996 1996
CUI: C0280783
Disease: Juvenile Pilocytic Astrocytoma
Juvenile Pilocytic Astrocytoma 		disease Neoplasms Neoplastic Process 38 2 0.010 None 1.000 1 2005 2005
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Stomatognathic Diseases Disease or Syndrome 41 14 0.010 None 1.000 1 2008 2008