Centrocecal scotoma
Symptom Information:
Symptom ID: | HPO:0000576 | ||
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 physiology(HPO:0012373) Abnormality of vision(HPO:0000504) Visual field defect(HPO:0001123) Scotoma(HPO:0000575) Centrocecal scotoma(HPO:0000576) MedDRA: |
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Database Frequency: | 6 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal dominant optic atrophy and congenital deafness | (Orphanet:3212) |
Autosomal dominant optic atrophy, classic type | (Orphanet:98673) |
Leber hereditary optic neuropathy | (Orphanet:104) |
Leber plus disease | (Orphanet:99718) |
OPTIC ATROPHY 1 | (OMIM:165500) |
[DEL] LEBER OPTIC ATROPHY | (OMIM:535000) |