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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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 Atrophies Optic Atrophies, Kjer-Type Optic Atrophy, Kjer-Type Optic Atrophy 1 Optic Atrophy 1s Kjer's Optic Atrophy Atrophy, Kjer's Optic Kjer Optic Atrophy Kjers Optic Atrophy Optic Atrophy, Kjer's Optic Atrophy, Hereditary, Autosomal Dominant Optic Atrophy, Juvenile Atrophies, Juvenile Optic Atrophy, Juvenile Optic Juvenile Optic Atrophies Juvenile Optic Atrophy Optic Atrophies, Juvenile Optic Atrophy, Kjer Type Autosomal Dominant Optic Atrophy Kjer Type Kjer Type Optic Atrophy Autosomal Dominant Optic Atrophy Optic Atrophy Type 1

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 related to "Optic Atrophy, Autosomal Dominant".

Below are MeSH descriptors whose meaning is more specific than "Optic Atrophy, Autosomal Dominant".

publications

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