Categorias DeCS
C05 Musculoskeletal Diseases .
C05.116 Bone Diseases .
C05.116.099 Bone Diseases, Developmental .
C05.116.099.708 Osteochondrodysplasias .
C05.116.099.708.685 Osteogenesis Imperfecta .
C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.140 Brain Damage, Chronic .
C10.228.140.140.254 Cerebral Palsy .
C10.228.140.163 Brain Diseases, Metabolic .
C10.228.140.163.100 Brain Diseases, Metabolic, Inborn .
C10.228.140.163.100.412 Leigh Disease .
C10.292 Cranial Nerve Diseases .
C10.292.700 Optic Nerve Diseases .
C10.292.700.225 Optic Atrophy .
C10.292.700.225.500 Optic Atrophies, Hereditary .
C10.292.700.225.500.400 Optic Atrophy, Hereditary, Leber .
C10.562 Neurocutaneous Syndromes .
C10.562.925 von Hippel-Lindau Disease .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.662 Optic Atrophies, Hereditary .
C10.574.500.662.400 Optic Atrophy, Hereditary, Leber .
C11 Eye Diseases .
C11.270 Eye Diseases, Hereditary .
C11.270.564 Optic Atrophies, Hereditary .
C11.270.564.400 Optic Atrophy, Hereditary, Leber .
C11.640 Optic Nerve Diseases .
C11.640.451 Optic Atrophy .
C11.640.451.451 Optic Atrophies, Hereditary .
C11.640.451.451.400 Optic Atrophy, Hereditary, Leber .
C12 Male Urogenital Diseases .
C12.777 Urologic Diseases .
C12.777.419 Kidney Diseases .
C12.777.419.815 Renal Tubular Transport, Inborn Errors .
C12.777.419.815.364 Dent Disease .
C13 Female Urogenital Diseases and Pregnancy Complications .
C13.351 Female Urogenital Diseases .
C13.351.968 Urologic Diseases .
C13.351.968.419 Kidney Diseases .
C13.351.968.419.815 Renal Tubular Transport, Inborn Errors .
C13.351.968.419.815.364 Dent Disease .
C14 Cardiovascular Diseases .
C14.907 Vascular Diseases .
C14.907.077 Angiomatosis .
C14.907.077.925 von Hippel-Lindau Disease .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.290 Eye Diseases, Hereditary .
C16.320.290.564 Optic Atrophies, Hereditary .
C16.320.290.564.400 Optic Atrophy, Hereditary, Leber .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.100 Dent Disease .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.630 Optic Atrophies, Hereditary .
C16.320.400.630.400 Optic Atrophy, Hereditary, Leber .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.412 Leigh Disease .
C16.320.565.202 Carbohydrate Metabolism, Inborn Errors .
C16.320.565.202.810 Pyruvate Metabolism, Inborn Errors .
C16.320.565.202.810.444 Leigh Disease .
C16.320.565.861 Renal Tubular Transport, Inborn Errors .
C16.320.565.861.271 Dent Disease .
C16.320.737 Osteogenesis Imperfecta .
C17 Skin and Connective Tissue Diseases .
C17.300 Connective Tissue Diseases .
C17.300.200 Collagen Diseases .
C17.300.200.540 Osteogenesis Imperfecta .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.412 Leigh Disease .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.412 Leigh Disease .
C18.452.648.202 Carbohydrate Metabolism, Inborn Errors .
C18.452.648.202.810 Pyruvate Metabolism, Inborn Errors .
C18.452.648.202.810.444 Leigh Disease .
C18.452.648.861 Renal Tubular Transport, Inborn Errors .
C18.452.648.861.271 Dent Disease .
C18.452.660 Mitochondrial Diseases .
C18.452.660.520 Leigh Disease .
C18.452.660.670 Optic Atrophy, Hereditary, Leber .
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| | Termos
Sinônimos e Históricos | Documentos
LILACS e MDL | | |
| Cerebral Palsy .
CP (Cerebral Palsy) .
Cerebral Palsy, Athetoid .
Cerebral Palsy, Atonic .
Cerebral Palsy, Congenital .
Cerebral Palsy, Diplegic, Infantile .
Cerebral Palsy, Dyskinetic .
Cerebral Palsy, Dystonic-Rigid .
Cerebral Palsy, Hypotonic .
Cerebral Palsy, Mixed .
Cerebral Palsy, Monoplegic, Infantile .
Cerebral Palsy, Quadriplegic, Infantile .
Cerebral Palsy, Rolandic Type .
Cerebral Palsy, Spastic .
Congenital Cerebral Palsy .
Diplegia, Spastic .
Infantile Cerebral Palsy, Diplegic .
Infantile Cerebral Palsy, Monoplegic .
Infantile Cerebral Palsy, Quadriplegic .
Little's Disease .
Monoplegic Infantile Cerebral Palsy .
Rolandic Type Cerebral Palsy .
Athetoid Cerebral Palsy .
Atonic Cerebral Palsy .
Cerebral Palsies, Athetoid .
Cerebral Palsies, Dyskinetic .
Cerebral Palsies, Dystonic-Rigid .
Cerebral Palsies, Monoplegic .
Cerebral Palsy, Dystonic Rigid .
Cerebral Palsy, Monoplegic .
Diplegias, Spastic .
Dyskinetic Cerebral Palsy .
Dystonic-Rigid Cerebral Palsies .
Dystonic-Rigid Cerebral Palsy .
Hypotonic Cerebral Palsies .
Hypotonic Cerebral Palsy .
Mixed Cerebral Palsies .
Mixed Cerebral Palsy .
Monoplegic Cerebral Palsies .
Spastic Cerebral Palsies .
Spastic Cerebral Palsy .
Spastic Diplegias .
Little Disease .
Spastic Diplegia .
Diplegic Infantile Cerebral Palsy .
Monoplegic Cerebral Palsy .
Quadriplegic Infantile Cerebral Palsy .
LITTLE'S DISEASE .
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| Leigh Disease .
Encephalomyelopathy, Subacute Necrotizing .
Encephalopathy, Subacute Necrotizing, Infantile .
Encephalopathy, Subacute Necrotizing, Juvenile .
Infantile Leigh Disease .
Infantile Subacute Necrotizing Encephalopathy .
Juvenile Leigh Disease .
Juvenile Subacute Necrotizing Encephalopathy .
Leigh Disease, Infantile .
Leigh Disease, Juvenile .
Leigh Syndrome .
Leigh's Disease .
Subacute Necrotizing Encephalomyelitis, Infantile .
Subacute Necrotizing Encephalomyelopathy .
Subacute Necrotizing Encephalopathy .
Subacute Necrotizing Encephalopathy, Infantile .
Subacute Necrotizing Encephalopathy, Juvenile .
Disease, Leigh's .
Encephalomyelitides, Subacute Necrotizing .
Encephalomyelopathies, Subacute Necrotizing .
Encephalopathies, Subacute Necrotizing .
Leighs Disease .
Necrotizing Encephalomyelitides, Subacute .
Necrotizing Encephalomyelitis, Subacute .
Necrotizing Encephalomyelopathies, Subacute .
Necrotizing Encephalomyelopathy, Subacute .
Necrotizing Encephalopathies, Subacute .
Necrotizing Encephalopathy, Subacute .
Subacute Necrotizing Encephalomyelitides .
Subacute Necrotizing Encephalomyelitis .
Subacute Necrotizing Encephalomyelopathies .
Subacute Necrotizing Encephalopathies .
Encephalomyelitis, Subacute Necrotizing .
Encephalopathy, Subacute Necrotizing .
CYTOCHROME OXIDASE DEFICIENCY DISEASE .
ENCEPHALOMYELOPATHY, SUBACUTE NECROTIZING .
0.61
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| von Hippel-Lindau Disease .
Angiomatosis Retinae .
Familial Cerebello-Retinal Angiomatosis .
Hippel-Lindau Disease .
Lindau's Disease .
VHL Syndrome .
von Hippel-Lindau Syndrome .
Angiomatoses, Familial Cerebello-Retinal .
Angiomatoses, Familial Cerebelloretinal .
Angiomatosis, Familial Cerebello-Retinal .
Angiomatosis, Familial Cerebelloretinal .
Cerebello-Retinal Angiomatoses, Familial .
Cerebello-Retinal Angiomatosis, Familial .
Cerebelloretinal Angiomatoses, Familial .
Familial Cerebello Retinal Angiomatosis .
Familial Cerebello-Retinal Angiomatoses .
Familial Cerebelloretinal Angiomatoses .
Familial Cerebelloretinal Angiomatosis .
Hippel Lindau Disease .
Lindau's Diseases .
Lindaus Disease .
Retinae, Angiomatosis .
Syndrome, VHL .
Syndrome, von Hippel-Lindau .
Syndromes, VHL .
VHL Syndromes .
von Hippel Lindau Disease .
von Hippel Lindau Syndrome .
Cerebelloretinal Angiomatosis, Familial .
Lindau Disease .
0.60
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| Optic Atrophy, Hereditary, Leber .
Hereditary Optic Neuroretinopathy .
Leber Hereditary Optic Neuropathy .
Leber Optic Atrophy .
Leber Optic Atrophy and Dystonia .
Leber's Disease .
Leber's Hereditary Optic Atrophy .
Leber's Hereditary Optic Neuropathy .
Leber's Optic Atrophy .
Leber's Optic Neuropathy .
Optic Atrophy, Leber Type .
Optic Atrophy, Leber, Hereditary .
Disease, Leber's .
Diseases, Leber's .
Hereditary Optic Neuroretinopathies .
Leber Disease .
Leber Optic Neuropathy .
Leber's Diseases .
Lebers Disease .
Lebers Optic Neuropathy .
Neuropathy, Leber's Optic .
Neuroretinopathies, Hereditary Optic .
Neuroretinopathy, Hereditary Optic .
Optic Atrophy, Leber .
Optic Neuropathy, Leber's .
Optic Neuroretinopathies, Hereditary .
Optic Neuroretinopathy, Hereditary .
Leber Hereditary Optic Atrophy .
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