serw-MX  [xml]  
 


    
 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 .
C10.228.140.163 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 .
C10.574 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 .
C11.270.516 Leber Congenital Amaurosis .
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 .
C11.768 Retinal Diseases .
C11.768.364 Leber Congenital Amaurosis .
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 .
C16.320.400 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 .
C16.320.737 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 .
C18.452.660 Mitochondrial Diseases .
C18.452.660.520 Leigh Disease .
C18.452.660.670 Optic Atrophy, Hereditary, Leber .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
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 .
1.00
 
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
 
Leber Congenital Amaurosis .
Amaurosis, Leber Congenital .
Congenital Amaurosis of Retinal Origin .
Congenital Retinal Blindness .
Dysgenesis Neuroepithelialis Retinae .
Hereditary Epithelial Dysplasia of Retina .
Hereditary Retinal Aplasia .
Heredoretinopathia Congenitalis .
Leber Abiotrophy .
Leber Congenital Tapetoretinal Degeneration .
Leber's Amaurosis .
Abiotrophies, Leber .
Abiotrophy, Leber .
Amauroses, Leber Congenital .
Amauroses, Leber's .
Amaurosis, Leber's .
Blindness, Congenital Retinal .
Blindnesses, Congenital Retinal .
Congenital Amauroses, Leber .
Congenital Amaurosis, Leber .
Congenital Retinal Blindnesses .
Leber Abiotrophies .
Leber Amaurosis .
Leber Congenital Amauroses .
Leber's Amauroses .
Lebers Amaurosis .
Retinal Blindnesses, Congenital .
0.60
 
Osteogenesis Imperfecta .
Brittle Bone Disease .
Lobstein's Disease .
Osteogenesis Imperfecta Tarda .
Osteogenesis Imperfecta with Blue Sclerae .
Osteogenesis Imperfecta, Type 1 .
Osteogenesis Imperfecta, Type I .
Disease, Lobstein .
Disease, Lobstein's .
Lobsteins Disease .
Ossiums, Fragilitas .
Osteogenesis Imperfecta Tardas .
Fragilitas Ossium .
Lobstein Disease .
LOBSTEIN'S DISEASE .
0.58