Optic Atrophies, Hereditary
"Optic Atrophies, Hereditary" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Hereditary conditions that feature progressive visual loss in association with optic atrophy. Relatively common forms include autosomal dominant optic atrophy (OPTIC ATROPHY, AUTOSOMAL DOMINANT) and Leber hereditary optic atrophy (OPTIC ATROPHY, HEREDITARY, LEBER).
| Descriptor ID |
D015418
|
| MeSH Number(s) |
C10.292.700.225.500 C10.574.500.662 C11.270.564 C11.640.451.451 C16.320.290.564 C16.320.400.630
|
| Concept/Terms |
Optic Atrophies, Hereditary- Optic Atrophies, Hereditary
- Optic Atrophy, Hereditary
- Hereditary Optic Atrophy
- Atrophies, Hereditary Optic
- Atrophy, Hereditary Optic
- Hereditary Optic Atrophies
|
Below are MeSH descriptors whose meaning is more general than "Optic Atrophies, Hereditary".
- Diseases [C]
- Nervous System Diseases [C10]
- Cranial Nerve Diseases [C10.292]
- Optic Nerve Diseases [C10.292.700]
- Optic Atrophy [C10.292.700.225]
- Optic Atrophies, Hereditary [C10.292.700.225.500]
- Neurodegenerative Diseases [C10.574]
- Heredodegenerative Disorders, Nervous System [C10.574.500]
- Optic Atrophies, Hereditary [C10.574.500.662]
- Eye Diseases [C11]
- Eye Diseases, Hereditary [C11.270]
- Optic Atrophies, Hereditary [C11.270.564]
- Optic Nerve Diseases [C11.640]
- Optic Atrophy [C11.640.451]
- Optic Atrophies, Hereditary [C11.640.451.451]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Eye Diseases, Hereditary [C16.320.290]
- Optic Atrophies, Hereditary [C16.320.290.564]
- Heredodegenerative Disorders, Nervous System [C16.320.400]
- Optic Atrophies, Hereditary [C16.320.400.630]
Below are MeSH descriptors whose meaning is more specific than "Optic Atrophies, Hereditary".
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