Optic Atrophy, Autosomal Dominant
"Optic Atrophy, Autosomal Dominant" 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.
Dominant optic atrophy is a hereditary optic neuropathy causing decreased visual acuity, color vision deficits, a centrocecal scotoma, and optic nerve pallor (Hum. Genet. 1998; 102: 79-86). Mutations leading to this condition have been mapped to the OPA1 gene at chromosome 3q28-q29. OPA1 codes for a dynamin-related GTPase that localizes to mitochondria.
| Descriptor ID |
D029241
|
| MeSH Number(s) |
C10.292.700.225.500.100 C10.574.500.662.100 C11.270.564.100 C11.640.451.451.100 C16.320.290.564.100 C16.320.400.630.100 C18.452.660.665
|
| Concept/Terms |
Optic Atrophy, Autosomal Dominant- Optic Atrophy, Autosomal Dominant
- Dominant Optic Atrophy
- Dominant Optic Atrophies
- Optic Atrophies, Dominant
- Optic Atrophy, Dominant
- Kjer-Type Optic Atrophy
- Atrophies, Kjer-Type Optic
- Atrophy, Kjer-Type Optic
- Kjer Type Optic Atrophy
- Kjer-Type Optic Atrophies
- Optic Atrophies, Kjer-Type
- Optic Atrophy, Kjer-Type
- Optic Atrophy, Kjer Type
- Optic Atrophy Type 1
- Optic Atrophy, Hereditary, Autosomal Dominant
- Optic Atrophy, Juvenile
- Atrophies, Juvenile Optic
- Atrophy, Juvenile Optic
- Juvenile Optic Atrophies
- Juvenile Optic Atrophy
- Optic Atrophies, Juvenile
- Autosomal Dominant Optic Atrophy
- Optic Atrophy 1
- Optic Atrophy 1s
|
Below are MeSH descriptors whose meaning is more general than "Optic Atrophy, Autosomal Dominant".
- 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]
- Optic Atrophy, Autosomal Dominant [C10.292.700.225.500.100]
- Neurodegenerative Diseases [C10.574]
- Heredodegenerative Disorders, Nervous System [C10.574.500]
- Optic Atrophies, Hereditary [C10.574.500.662]
- Optic Atrophy, Autosomal Dominant [C10.574.500.662.100]
- Eye Diseases [C11]
- Eye Diseases, Hereditary [C11.270]
- Optic Atrophies, Hereditary [C11.270.564]
- Optic Atrophy, Autosomal Dominant [C11.270.564.100]
- Optic Nerve Diseases [C11.640]
- Optic Atrophy [C11.640.451]
- Optic Atrophies, Hereditary [C11.640.451.451]
- Optic Atrophy, Autosomal Dominant [C11.640.451.451.100]
- 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]
- Optic Atrophy, Autosomal Dominant [C16.320.290.564.100]
- Heredodegenerative Disorders, Nervous System [C16.320.400]
- Optic Atrophies, Hereditary [C16.320.400.630]
- Optic Atrophy, Autosomal Dominant [C16.320.400.630.100]
- Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
- Mitochondrial Diseases [C18.452.660]
- Optic Atrophy, Autosomal Dominant [C18.452.660.665]
Below are MeSH descriptors whose meaning is more specific than "Optic Atrophy, Autosomal Dominant".
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