loading...| Preferred Name | Leber hereditary optic neuropathy | |
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| Definitions |
(LHON): A maternally inherited disease resulting in acute or subacute loss of central vision, due to optic nerve dysfunction. Cardiac conduction defects and neurological defects have also been described in some patients. LHON results from primary mitochondrial DNA mutations affecting the respiratory chain complexes. |
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| ID |
http://purl.obolibrary.org/obo/OMIM_535000 |
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| definition |
(LHON): A maternally inherited disease resulting in acute or subacute loss of central vision, due to optic nerve dysfunction. Cardiac conduction defects and neurological defects have also been described in some patients. LHON results from primary mitochondrial DNA mutations affecting the respiratory chain complexes. |
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| has_obo_namespace |
cell_cycle_ontology |
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| id |
OMIM:535000 |
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| label |
Leber hereditary optic neuropathy |
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| notation |
OMIM:535000 |
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| prefLabel |
Leber hereditary optic neuropathy |
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