Leber optic atrophy
Symptom Information:
Symptom ID: | HPO:0001112 | ||||
Synonyms: |
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Quality: | |||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the eye(HPO:0000478) Abnormal eye morphology(HPO:0012372) Abnormality of the globe(HPO:0012374) Abnormality of the posterior segment of the globe(HPO:0004329) Abnormality of the fundus(HPO:0001098) Abnormality of the optic nerve(HPO:0000587) Leber optic atrophy(HPO:0001112) Abnormality of the retina(HPO:0000479) Leber optic atrophy(HPO:0001112) MedDRA: |
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Database Frequency: | 9 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
COMPLEX I, SUBUNIT ND2 | (OMIM:516001) |
COMPLEX I, SUBUNIT ND5 | (OMIM:516005) |
COMPLEX I, SUBUNIT ND6 | (OMIM:516006) |
COMPLEX IV, CYTOCHROME c OXIDASE SUBUNIT I | (OMIM:516030) |
CYTOCHROME b OF COMPLEX III | (OMIM:516020) |
CYTOCHROME c OXIDASE III | (OMIM:516050) |
LEBER OPTIC ATROPHY AND DYSTONIA | (OMIM:500001) |
Leber hereditary optic neuropathy | (Orphanet:104) |
[DEL] LEBER OPTIC ATROPHY | (OMIM:535000) |