serw-MX  [xml]  

 DeCS Categories

C01 Bacterial Infections and Mycoses .
C01.539 Infection .
C01.539.100 Arthritis, Infectious .
C01.539.100.500 Arthritis, Reactive .
C05 Musculoskeletal Diseases .
C05.116 Bone Diseases .
C05.116.900 Spinal Diseases .
C05.116.900.853 Spondylitis .
C05.116.900.853.625 Spondylarthritis .
C05.116.900.853.625.800 Spondylarthropathies .
C05.116.900.853.625.800.637 Arthritis, Reactive .
C05.550 Joint Diseases .
C05.550.114 Arthritis .
C05.550.114.099 Arthritis, Infectious .
C05.550.114.099.500 Arthritis, Reactive .
C05.550.114.865 Spondylarthritis .
C05.550.114.865.800 Spondylarthropathies .
C05.550.114.865.800.637 Arthritis, Reactive .
C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.163 Brain Diseases, Metabolic .
C10. Brain Diseases, Metabolic, Inborn .
C10. Hereditary Central Nervous System Demyelinating Diseases .
C10. Pelizaeus-Merzbacher Disease .
C10.228.140.695 Leukoencephalopathies .
C10.228.140.695.625 Hereditary Central Nervous System Demyelinating Diseases .
C10.228.140.695.625.775 Pelizaeus-Merzbacher Disease .
C10.228.662 Movement Disorders .
C10.314 Demyelinating Diseases .
C10.314.400 Hereditary Central Nervous System Demyelinating Diseases .
C10.314.400.775 Pelizaeus-Merzbacher Disease .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.906 Pelizaeus-Merzbacher Disease .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.362 Hereditary Central Nervous System Demyelinating Diseases .
C16.320.565.189.362.775 Pelizaeus-Merzbacher Disease .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.362 Hereditary Central Nervous System Demyelinating Diseases .
C18.452.132.100.362.775 Pelizaeus-Merzbacher Disease .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.362 Hereditary Central Nervous System Demyelinating Diseases .
C18.452.648.189.362.775 Pelizaeus-Merzbacher Disease .
D08 Enzymes and Coenzymes .
D08.811 Enzymes .
D08.811.277 Hydrolases .
D08.811.277.352 Esterases .
D08.811.277.352.650 Phosphoric Monoester Hydrolases .
D08.811.277.352.650.775 Protein Tyrosine Phosphatases .
D08.811.277.352.650.775.300 Protein Tyrosine Phosphatases, Non-Receptor .
D12 Amino Acids, Peptides, and Proteins .
D12.644 Peptides .
D12.644.360 Intracellular Signaling Peptides and Proteins .
D12.644.360.585 Protein Tyrosine Phosphatases, Non-Receptor .
D12.776 Proteins .
D12.776.476 Intracellular Signaling Peptides and Proteins .
D12.776.476.564 Protein Tyrosine Phosphatases, Non-Receptor .
M01 Persons .
M01.060 Age Groups .
M01.060.703 Infant .
M01.060.703.520 Infant, Newborn .
M01.060.703.520.500 Infant, Postmature .
 Synonyms & Historicals
Movement Disorders .
Movement Disorder Syndromes .
Dyskinesia Syndrome .
Movement Disorder .
Movement Disorder Syndrome .
Etat Marbre .
Status Marmoratus .
Dyskinesia Syndromes .
Syndromes which feature DYSKINESIAS as a cardinal manifestation of the disease process. Included in this category are degenerative, hereditary, post-infectious, medication-induced, post-inflammatory, and post-traumatic conditions. .
Infant, Postmature .
Infants, Postmature .
Postmature Infant .
Postmature Infants .
An infant born at or after 42 weeks of gestation. .
Pelizaeus-Merzbacher Disease .
Adult Pelizaeus-Merzbacher Disease .
Atypical Pelizaeus-Merzbacher Disease .
Classic Pelizaeus-Merzbacher Disease .
Leukodystrophy, Hypomyelinating, 1 .
Pelizaeus-Merzbacher Brain Sclerosis .
Pelizaeus-Merzbacher Disease, Adult .
Pelizaeus-Merzbacher Disease, Atypical .
Pelizaeus-Merzbacher Disease, Classic .
Pelizaeus-Merzbacher Disease, Transitional .
Pelizaeus-Merzbacher Sclerosis, Brain .
Transitional Pelizaeus-Merzbacher Disease .
Adult Pelizaeus Merzbacher Disease .
Atypical Pelizaeus Merzbacher Disease .
Brain Pelizaeus-Merzbacher Sclerosis .
Brain Sclerosis, Pelizaeus-Merzbacher .
Classic Pelizaeus Merzbacher Disease .
Cockayne Pelizaeus Merzbacher Disease .
Pelizaeus Merzbacher Brain Sclerosis .
Pelizaeus Merzbacher Disease .
Pelizaeus Merzbacher Disease, Adult .
Pelizaeus Merzbacher Disease, Atypical .
Pelizaeus Merzbacher Disease, Classic .
Pelizaeus Merzbacher Disease, Transitional .
Pelizaeus Merzbacher Sclerosis, Brain .
Transitional Pelizaeus Merzbacher Disease .
Cockayne-Pelizaeus-Merzbacher Disease .
A rare, slowly progressive disorder of myelin formation. Subtypes are referred to as classic, congenital, transitional, and adult forms of this disease. The classic form is X-chromosome linked, has its onset in infancy and is associated with a mutation of the proteolipid protein gene. Clinical manifestations include TREMOR, spasmus nutans, roving eye movements, ATAXIA, spasticity, and NYSTAGMUS, CONGENITAL. Death occurs by the third decade of life. The congenital form has similar characteristics but presents early in infancy and features rapid disease progression. Transitional and adult subtypes have a later onset and less severe symptomatology. Pathologic features include patchy areas of demyelination with preservation of perivascular islands (trigoid appearance). (From Menkes, Textbook of Child Neurology, 5th ed, p190) .
Protein Tyrosine Phosphatases, Non-Receptor .
Non-Transmembrane Protein Tyrosine Phosphatases .
Non Transmembrane Protein Tyrosine Phosphatases .
Protein Tyrosine Phosphatases, Non Receptor .
A subcategory of protein tyrosine phosphatases that occur in the CYTOPLASM. Many of the proteins in this category play a role in intracellular signal transduction. .
Arthritis, Reactive .
Arthritis, Post-Infectious .
Post-Infectious Arthritis .
Postinfectious Arthritis .
Reactive Arthritis .
Reiter Disease .
Reiter Syndrome .
Reiter's Disease .
Arthritides, Post-Infectious .
Arthritides, Postinfectious .
Arthritides, Reactive .
Arthritis, Post Infectious .
Disease, Reiter .
Disease, Reiter's .
Post Infectious Arthritis .
Post-Infectious Arthritides .
Postinfectious Arthritides .
Reactive Arthritides .
Reiters Disease .
Syndrome, Reiter .
Arthritis, Postinfectious .
Reiter's Disease .
Reiter Disease .
Reiter Syndrome .
An aseptic, inflammatory arthritis developing secondary to a primary extra-articular infection, most typically of the GASTROINTESTINAL TRACT or UROGENITAL SYSTEM. The initiating trigger pathogens are usually SHIGELLA; SALMONELLA; YERSINIA; CAMPYLOBACTER; or CHLAMYDIA TRACHOMATIS. Reactive arthritis is strongly associated with HLA-B27 ANTIGEN. .