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 DeCS Categories

C05 Musculoskeletal Diseases .
C05.116 Bone Diseases .
C05.116.900 Spinal Diseases .
C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.252 Cerebellar Diseases .
C10.228.140.252.700 Spinocerebellar Degenerations .
C10.228.854 Spinal Cord Diseases .
C10.228.854.787 Spinocerebellar Degenerations .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.825 Spinocerebellar Degenerations .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.780 Spinocerebellar Degenerations .
C23 Pathological Conditions, Signs and Symptoms .
C23.550 Pathologic Processes .
C23.550.288 Disease .
F03 Mental Disorders .
F03.875 Somatoform Disorders .
HP1 Homeopathy .
HP1.007 Homeopathic Philosophy .
HP1.007.262 Patients .
HP1.007.262.808 Disease .
HP2 Homeopathic Clinics .
HP2.029 Disease .
SP5 Epidemiology and Biostatistics .
SP5.001 Epidemiology .
SP5.001.002 Health-Disease Process .
SP5.001.002.013 Disease .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Spinal Diseases .
Disease, Spinal .
Diseases, Spinal .
Spinal Disease .
Diseases involving the SPINE. .
1.00
30617098
 
Spinal Cord Diseases .
Spinal Cord Disorders .
Myelopathies .
Spinal Cord Disease .
Spinal Cord Disorder .
Myelopathy .
Pathologic conditions which feature SPINAL CORD damage or dysfunction, including disorders involving the meninges and perimeningeal spaces surrounding the spinal cord. Traumatic injuries, vascular diseases, infections, and inflammatory/autoimmune processes may affect the spinal cord. .
0.79
20610565
 
Somatoform Disorders .
Medically Unexplained Syndrome .
Medically Unexplained Syndromes .
Disorder, Somatoform .
Disorders, Somatization .
Disorders, Somatoform .
Somatization Disorders .
Somatoform Disorder .
Syndrome, Briquet .
Syndrome, Medically Unexplained .
Syndromes, Medically Unexplained .
Unexplained Syndrome, Medically .
Unexplained Syndromes, Medically .
Diseases of the Spirit .
Spiritual Disease .
Spiritual Diseases .
Briquet Syndrome .
Pain Disorder .
Somatization Disorder .
Disorders having the presence of physical symptoms that suggest a general medical condition but that are not fully explained by another medical condition, by the direct effects of a substance, or by another mental disorder. The MEDICALLY UNEXPLAINED SYMPTOMS must cause clinically significant distress or impairment in social, occupational, or other areas of functioning. In contrast to FACTITIOUS DISORDERS and MALINGERING, the physical symptoms are not under voluntary control. (APA, DSM-V) .
0.72
1928558
 
Spinocerebellar Degenerations .
Early Onset Cerebellar Ataxia .
Familial Spinocerebellar Degenerations .
Garland-Moorhouse Syndrome .
Hereditary Oligophrenic Cerebello-Lental Degeneration .
Hereditary Spinocerebellar Degenerations .
Inherited Spinocerebellar Degenerations .
Late Onset Cerebellar Ataxia .
Marie's Cerebellar Ataxia .
Marinesco-Garland Syndrome .
Marinesco-Sjogren Syndrome-Hypergonadotrophic Hypogonadism .
Marinesco-Sjogren Syndrome-Myopathy .
Marinesco-Sjogren-Garland Syndrome .
Marinesco-Sjögren Syndrome .
Spino Cerebellar Degenerations .
Spino-Cerebellar Degenerations .
Spinocerebellar Diseases .
Ataxia, Hereditary .
Cerebellar Ataxia, Marie .
Cerebellar Ataxia, Marie's .
Cerebellar Degeneration, Primary .
Corticostriatal Spinal Degeneration .
Corticostriatal-Spinal Degenerations .
Degeneration, Corticostriatal-Spinal .
Degeneration, Familial Spinocerebellar .
Degeneration, Hereditary Spinocerebellar .
Degeneration, Inherited Spinocerebellar .
Degeneration, Primary Cerebellar .
Degeneration, Spino Cerebellar .
Degeneration, Spino-Cerebellar .
Degeneration, Spinocerebellar .
Degenerations, Corticostriatal-Spinal .
Degenerations, Familial Spinocerebellar .
Degenerations, Hereditary Spinocerebellar .
Degenerations, Inherited Spinocerebellar .
Degenerations, Primary Cerebellar .
Degenerations, Spino Cerebellar .
Degenerations, Spinocerebellar .
Familial Spinocerebellar Degeneration .
Garland Moorhouse Syndrome .
Hereditary Ataxia .
Hereditary Ataxias .
Hereditary Oligophrenic Cerebello Lental Degeneration .
Hereditary Spinocerebellar Degeneration .
Hypogonadism, Marinesco-Sjogren Syndrome-Hypergonadotrophic .
Inherited Spinocerebellar Degeneration .
Marinesco Garland Syndrome .
Marinesco Sjogren Garland Syndrome .
Marinesco Sjogren Syndrome .
Marinesco Sjogren Syndrome Hypergonadotrophic Hypogonadism .
Marinesco Sjogren Syndrome Myopathy .
Marinesco Sjögren Syndrome .
Primary Cerebellar Degeneration .
Primary Cerebellar Degenerations .
Spino Cerebellar Degeneration .
Spino-Cerebellar Degeneration .
Spinocerebellar Degeneration, Familial .
Spinocerebellar Degeneration, Hereditary .
Spinocerebellar Degeneration, Inherited .
Spinocerebellar Degenerations, Familial .
Spinocerebellar Degenerations, Hereditary .
Spinocerebellar Degenerations, Inherited .
Spinocerebellar Disease .
Syndrome, Garland-Moorhouse .
Syndrome, Marinesco-Garland .
Syndrome, Marinesco-Sjogren .
Syndrome, Marinesco-Sjogren-Garland .
Syndrome, Marinesco-Sjögren .
Syndrome-Hypergonadotrophic Hypogonadism, Marinesco-Sjogren .
Syndrome-Myopathy, Marinesco-Sjogren .
Ataxias, Hereditary .
Marinesco-Sjogren Syndrome .
Spinocerebellar Degeneration .
Cerebellar Ataxia, Early Onset .
Cerebellar Ataxia, Late Onset .
Cerebellar Degenerations, Primary .
Corticostriatal-Spinal Degeneration .
Marie Cerebellar Ataxia .
A heterogenous group of degenerative syndromes marked by progressive cerebellar dysfunction either in isolation or combined with other neurologic manifestations. Sporadic and inherited subtypes occur. Inheritance patterns include autosomal dominant, autosomal recessive, and X-linked. .
0.70
321699
 
Disease .
Diseases .
Illness .
Disease Concept Evolution .
A definite pathologic process with a characteristic set of signs and symptoms. It may affect the whole body or any of its parts, and its etiology, pathology, and prognosis may be known or unknown. .
0.68
81817203