Leber optic atrophy

Symptom Information:

Symptom ID: HPO:0001112
Synonyms:
Leber optic atrophy features [HPO:0001112]
Quality:
Cross references:
Is a (Direct Parents):
HPO         Abnormality of the retina
HPO         Abnormality of the optic nerve
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 retina(HPO:0000479)
                         Leber optic atrophy(HPO:0001112)
                      Abnormality of the optic nerve(HPO:0000587)
                         Leber optic atrophy(HPO:0001112)
MedDRA:
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)