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DeCS
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Descriptor Inglés:
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Optic Atrophy, Hereditary, Leber
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Descriptor Español:
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atrofia óptica hereditaria de Leber
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Descriptor Portugués:
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Atrofia Óptica Hereditária de Leber
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Sinónimos Inglés:
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Disease, Leber's
Diseases, Leber's
Hereditary Optic Neuroretinopathies
Hereditary Optic Neuroretinopathy
Leber Disease
Leber Hereditary Optic Atrophy
Leber Hereditary Optic Neuropathy
Leber Optic Atrophy
Leber Optic Atrophy and Dystonia
Leber Optic Neuropathy
Leber's Disease
Leber's Diseases
Leber's Hereditary Optic Atrophy
Leber's Hereditary Optic Neuropathy
Leber's Optic Atrophy
Leber's Optic Neuropathy
Lebers Disease
Lebers Optic Neuropathy
Neuropathy, Leber's Optic
Neuroretinopathies, Hereditary Optic
Neuroretinopathy, Hereditary Optic
Optic Atrophy, Leber
Optic Atrophy, Leber Type
Optic Atrophy, Leber, Hereditary
Optic Neuropathy, Leber's
Optic Neuroretinopathies, Hereditary
Optic Neuroretinopathy, Hereditary
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Categoría:
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C10.292.700.225.500.400
C10.574.500.662.400
C11.270.564.400
C11.640.451.451.400
C16.320.290.564.400
C16.320.400.630.400
C18.452.660.670
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Definición Inglés:
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A maternally linked genetic disorder that presents in mid-life as acute or subacute central vision loss leading to central scotoma and blindness. The disease has been associated with missense mutations in the mtDNA, in genes for Complex I, III, and IV polypeptides, that can act autonomously or in association with each other to cause the disease. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/Omim/, MIM#535000 (April 17, 2001)) |
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Nota Histórica Inglés:
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2002; use OPTIC ATROPHIES, HEREDITARY 1999-2001
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Calificadores Permitidos Inglés:
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Número del Registro:
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36011
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Identificador Único:
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D029242
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Ocurrencia en la BVS:
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Similar:
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DeCS
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