Categorias DeCS
C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.163 Brain Diseases, Metabolic .
C10.228.140.163.100 Brain Diseases, Metabolic, Inborn .
C10.228.140.163.100.168 Cerebral Amyloid Angiopathy, Familial .
C10.228.140.252 Cerebellar Diseases .
C10.228.140.252.190 Cerebellar Ataxia .
C10.228.140.252.190.530 Spinocerebellar Ataxias .
C10.228.140.252.700 Spinocerebellar Degenerations .
C10.228.140.252.700.700 Spinocerebellar Ataxias .
C10.228.140.300 Cerebrovascular Disorders .
C10.228.140.300.275 Cerebral Small Vessel Diseases .
C10.228.140.300.275.311 Cerebral Amyloid Angiopathy, Familial .
C10.228.140.300.510 Intracranial Arterial Diseases .
C10.228.140.300.510.200 Cerebral Arterial Diseases .
C10.228.140.300.510.200.200 Cerebral Amyloid Angiopathy .
C10.228.140.300.510.200.200.160 Cerebral Amyloid Angiopathy, Familial .
C10.228.854 Spinal Cord Diseases .
C10.228.854.787 Spinocerebellar Degenerations .
C10.228.854.787.875 Spinocerebellar Ataxias .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.825 Spinocerebellar Degenerations .
C10.574.500.825.700 Spinocerebellar Ataxias .
C10.597 Neurologic Manifestations .
C10.597.350 Dyskinesias .
C10.597.350.090 Ataxia .
C10.597.350.090.500 Cerebellar Ataxia .
C10.597.350.090.500.530 Spinocerebellar Ataxias .
C14 Cardiovascular Diseases .
C14.907 Vascular Diseases .
C14.907.253 Cerebrovascular Disorders .
C14.907.253.329 Cerebral Small Vessel Diseases .
C14.907.253.329.311 Cerebral Amyloid Angiopathy, Familial .
C14.907.253.560 Intracranial Arterial Diseases .
C14.907.253.560.200 Cerebral Arterial Diseases .
C14.907.253.560.200.200 Cerebral Amyloid Angiopathy .
C14.907.253.560.200.200.160 Cerebral Amyloid Angiopathy, Familial .
C15 Hemic and Lymphatic Diseases .
C15.378 Hematologic Diseases .
C15.378.100 Blood Coagulation Disorders .
C15.378.100.832 Thrombocythemia, Essential .
C15.378.140 Blood Platelet Disorders .
C15.378.140.860 Thrombocytosis .
C15.378.140.860.800 Thrombocythemia, Essential .
C15.378.190 Bone Marrow Diseases .
C15.378.190.636 Myeloproliferative Disorders .
C15.378.190.636.860 Thrombocytosis .
C15.378.190.636.860.800 Thrombocythemia, Essential .
C15.378.463 Hemorrhagic Disorders .
C15.378.463.825 Thrombocythemia, Essential .
C15.378.553 Leukocyte Disorders .
C15.378.553.774 Phagocyte Bactericidal Dysfunction .
C15.378.553.774.600 Job Syndrome .
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 .
C16.320.400.780.875 Spinocerebellar Ataxias .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.176 Amyloidosis, Familial .
C16.320.565.176.160 Cerebral Amyloid Angiopathy, Familial .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.168 Cerebral Amyloid Angiopathy, Familial .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.168 Cerebral Amyloid Angiopathy, Familial .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.176 Amyloidosis, Familial .
C18.452.648.176.160 Cerebral Amyloid Angiopathy, Familial .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.168 Cerebral Amyloid Angiopathy, Familial .
C18.452.845 Proteostasis Deficiencies .
C18.452.845.500 Amyloidosis .
C18.452.845.500.075 Amyloidosis, Familial .
C18.452.845.500.075.160 Cerebral Amyloid Angiopathy, Familial .
C18.452.845.500.100 Cerebral Amyloid Angiopathy .
C18.452.845.500.100.160 Cerebral Amyloid Angiopathy, Familial .
C20 Immune System Diseases .
C20.673 Immunologic Deficiency Syndromes .
C20.673.774 Phagocyte Bactericidal Dysfunction .
C20.673.774.600 Job Syndrome .
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| | Termos
Sinônimos e Históricos | Documentos
LILACS e MDL | | |
| Cerebral Amyloid Angiopathy, Familial .
Amyloidosis VI .
Amyloidosis, Cerebroarterial, Icelandic Type .
Autosomal Dominant Cerebrovascular Amyloidosis .
Cerebral Amyloid Angiopathy, Cst3-Related .
Cerebral Amyloid Angiopathy, Genetic .
Cerebral Amyloid Angiopathy, Hereditary .
Cerebral Hemorrhage, Hereditary, With Amyloidosis .
Familial Cerebral Amyloid Angiopathy .
HCHWA .
Hereditary Cerebral Amyloid Angiopathy .
Hereditary Cerebral Amyloid Angiopathy, Icelandic Type .
Hereditary Cerebral Hemorrhage With Amyloidosis .
Icelandic Type Amyloidosis .
Icelandic Type Hereditary Cerebral Amyloid Angiopathy .
Amyloidosis VIs .
Amyloidosis, Icelandic Type .
Cerebral Amyloid Angiopathy, Cst3 Related .
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| Spinocerebellar Ataxias .
Autosomal Dominant Cerebellar Ataxia, Type II .
Cerebellar Degeneration with Slow Eye Movements .
Cerebelloparenchymal Disorder I .
Dominantly-Inherited Spinocerebellar Ataxias .
Menzel Type OPCA .
OPCA with Macular Degeneration and External Ophthalmoplegia .
OPCA with Retinal Degeneration .
Olivopontocerebellar Atrophy 2 .
Olivopontocerebellar Atrophy I .
Olivopontocerebellar Atrophy II .
Olivopontocerebellar Atrophy III .
Olivopontocerebellar Atrophy IV .
Olivopontocerebellar Atrophy, Holguin Type .
SCA1 22058 .
Schut-Haymaker Type OPCA .
Spinocerebellar Ataxia 1 .
Spinocerebellar Ataxia 2 .
Spinocerebellar Ataxia 4 .
Spinocerebellar Ataxia 5 .
Spinocerebellar Ataxia 6 .
Spinocerebellar Ataxia 7 .
Spinocerebellar Ataxia with Slow Eye Movements .
Spinocerebellar Ataxia, Autosomal Dominant, with Sensory Axonal Neuropathy .
Spinocerebellar Ataxia, Cuban Type .
Spinocerebellar Ataxia-1 .
Spinocerebellar Ataxia-2 .
Spinocerebellar Ataxia-4 .
Spinocerebellar Ataxia-5 .
Spinocerebellar Ataxia-6 .
Spinocerebellar Ataxia-7 .
Spinocerebellar Ataxias, Dominantly-Inherited .
Spinocerebellar Atrophy 2 .
Spinocerebellar Atrophy I .
Spinocerebellar Atrophy II .
Spinocerebellar Degeneration with Slow Eye Movements .
Type 1 Spinocerebellar Ataxia .
Type 2 Spinocerebellar Ataxia .
Type 4 Spinocerebellar Ataxia .
Type 5 Spinocerebellar Ataxia .
Type 6 Spinocerebellar Ataxia .
Type 7 Spinocerebellar Ataxia .
Wadia Swami Syndrome .
Wadia-Swami Syndrome .
Ataxia 1, Spinocerebellar .
Ataxia 2, Spinocerebellar .
Ataxia 2s, Spinocerebellar .
Ataxia 4, Spinocerebellar .
Ataxia 4s, Spinocerebellar .
Ataxia 5, Spinocerebellar .
Ataxia 5s, Spinocerebellar .
Ataxia 6, Spinocerebellar .
Ataxia 6s, Spinocerebellar .
Ataxia 7, Spinocerebellar .
Ataxia 7s, Spinocerebellar .
Ataxia, Dominantly-Inherited Spinocerebellar .
Ataxia, Spinocerebellar .
Ataxias, Dominantly-Inherited Spinocerebellar .
Ataxias, Spinocerebellar .
Atrophies, Spinocerebellar .
Atrophy 2, Olivopontocerebellar .
Atrophy 2, Spinocerebellar .
Atrophy 2s, Olivopontocerebellar .
Atrophy 2s, Spinocerebellar .
Atrophy I, Olivopontocerebellar .
Atrophy I, Spinocerebellar .
Atrophy II, Olivopontocerebellar .
Atrophy II, Spinocerebellar .
Atrophy III, Olivopontocerebellar .
Atrophy IIs, Olivopontocerebellar .
Atrophy IIs, Spinocerebellar .
Atrophy IV, Olivopontocerebellar .
Atrophy IVs, Olivopontocerebellar .
Atrophy, Spinocerebellar .
Cerebelloparenchymal Disorder Is .
Dominantly Inherited Spinocerebellar Ataxias .
Dominantly-Inherited Spinocerebellar Ataxia .
II, Olivopontocerebellar Atrophy .
II, Spinocerebellar Atrophy .
IIs, Olivopontocerebellar Atrophy .
IIs, Spinocerebellar Atrophy .
OPCA, Menzel Type .
OPCA, Schut-Haymaker Type .
Olivopontocerebellar Atrophy 2s .
Olivopontocerebellar Atrophy IIIs .
Olivopontocerebellar Atrophy IIs .
Olivopontocerebellar Atrophy IVs .
Olivopontocerebellar Atrophy Is .
SCA1s .
Schut Haymaker Type OPCA .
Spinocerebellar Ataxia .
Spinocerebellar Ataxia 1s .
Spinocerebellar Ataxia 2s .
Spinocerebellar Ataxia 4s .
Spinocerebellar Ataxia 5s .
Spinocerebellar Ataxia 6s .
Spinocerebellar Ataxia 7s .
Spinocerebellar Ataxia, Dominantly-Inherited .
Spinocerebellar Ataxias, Dominantly Inherited .
Spinocerebellar Atrophy .
Spinocerebellar Atrophy 2s .
Spinocerebellar Atrophy IIs .
Spinocerebellar Atrophy Is .
Swami Syndrome, Wadia .
Syndrome, Wadia Swami .
Syndrome, Wadia-Swami .
Spinocerebellar Ataxia Type 1 .
Spinocerebellar Ataxia Type 2 .
Spinocerebellar Ataxia Type 4 .
Spinocerebellar Ataxia Type 5 .
Spinocerebellar Ataxia Type 6 .
Spinocerebellar Ataxia Type 7 .
Spinocerebellar Atrophies .
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| Job Syndrome .
Buckley Syndrome .
HIE Syndrome .
HIES, Autosomal Dominant .
Hyper-IgE Recurrent Infection Syndrome, Autosomal Recessive .
Hyper-IgE Syndrome .
Hyper-IgE Syndrome, Autosomal Dominant .
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant .
Hyperimmunoglobulin E, Recurrent Infection Syndrome .
Hyperimmunoglobulinemia E Syndrome .
Job-Buckley Syndrome .
Autosomal Dominant HIES .
Autosomal Dominant HIESs .
Autosomal Recessive HIES .
Autosomal Recessive HIESs .
Buckley Syndromes .
HIE Syndromes .
HIESs, Autosomal Dominant .
HIESs, Autosomal Recessive .
Hyper IgE Recurrent Infection Syndrome, Autosomal Recessive .
Hyper IgE Syndrome .
Hyper IgE Syndrome, Autosomal Dominant .
Hyper IgE Syndrome, Autosomal Recessive .
Hyper Immunoglobulin E Syndrome, Autosomal Dominant .
Hyper Immunoglobulin E Syndrome, Autosomal Recessive .
Hyper-IgE Syndromes .
Hyperimmunoglobulin E Recurrent Infection Syndrome .
Hyperimmunoglobulinemia E Syndromes .
Job Buckley Syndrome .
Job Syndromes .
Job-Buckley Syndromes .
Jobs Syndrome .
Syndrome, Buckley .
Syndrome, HIE .
Syndrome, Hyper-IgE .
Syndrome, Hyperimmunoglobulinemia E .
Syndrome, Job .
Syndrome, Job's .
Syndrome, Job-Buckley .
Syndromes, Buckley .
Syndromes, HIE .
Syndromes, Hyperimmunoglobulinemia E .
Syndromes, Job .
Syndromes, Job-Buckley .
HIES, Autosomal Recessive .
Hyper-IgE Syndrome, Autosomal Recessive .
Hyper-Immunoglobulin E Syndrome, Autosomal Recessive .
Hyperimmunoglobulin E-Recurrent Infection Syndrome .
Job's Syndrome .
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| Thrombocythemia, Essential .
Primary Thrombocythemia .
Thrombocytosis, Autosomal Dominant .
Thrombocytosis, Primary .
Autosomal Dominant Thrombocytoses .
Autosomal Dominant Thrombocytosis .
Dominant Thrombocytoses, Autosomal .
Dominant Thrombocytosis, Autosomal .
Essential Thrombocythemia .
Essential Thrombocythemias .
Hemorrhagic Thrombocythemias .
Idiopathic Thrombocythemia .
Idiopathic Thrombocythemias .
Primary Thrombocythemias .
Primary Thrombocytoses .
Primary Thrombocytosis .
Thrombocythemias, Essential .
Thrombocythemias, Hemorrhagic .
Thrombocythemias, Idiopathic .
Thrombocythemias, Primary .
Thrombocytoses, Autosomal Dominant .
Thrombocytoses, Primary .
Thrombocythemia, Hemorrhagic .
Thrombocythemia, Idiopathic .
Thrombocythemia, Primary .
Hemorrhagic Thrombocythemia .
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| Cerebrovascular Disorders .
Cerebrovascular Diseases .
Cerebrovascular Insufficiency .
Cerebrovascular Occlusion .
Brain Vascular Disorder .
Cerebrovascular Disease .
Cerebrovascular Disorder .
Cerebrovascular Insufficiencies .
Cerebrovascular Occlusions .
Disease, Cerebrovascular .
Diseases, Cerebrovascular .
Insufficiencies, Cerebrovascular .
Insufficiency, Cerebrovascular .
Intracranial Vascular Disease .
Intracranial Vascular Diseases .
Intracranial Vascular Disorder .
Occlusion, Cerebrovascular .
Occlusions, Cerebrovascular .
Vascular Disease, Intracranial .
Vascular Disorder, Brain .
Vascular Disorder, Intracranial .
Vascular Disorders, Brain .
Vascular Disorders, Intracranial .
Brain Vascular Disorders .
Intracranial Vascular Disorders .
Vascular Diseases, Intracranial .
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