Scotoma
Symptom Information:
Symptom ID: | HPO:0000575 | ||||||||||||||||||||||||||||||||
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) MedDRA: Eye disorders(MedDRA:10015919) Vision disorders(MedDRA:10047518) Visual field disorders(MedDRA:10047559) Scotoma(HPO:0000575) |
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Database Frequency: | 11 / 7739 | ||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Autosomal recessive spastic paraplegia type 55 | (Orphanet:320375) |
Bietti crystalline dystrophy | (Orphanet:41751) |
Cone dystrophy with supernormal rod response | (Orphanet:209932) |
Familial vascular leukoencephalopathy | (Orphanet:36383) |
Late-onset retinal degeneration | (Orphanet:67042) |
MELAS | (Orphanet:550) |
NEWFOUNDLAND ROD-CONE DYSTROPHY | (OMIM:607476) |
Posterior column ataxia - retinitis pigmentosa | (Orphanet:88628) |
RETINITIS PIGMENTOSA 18 | (OMIM:601414) |
RETINITIS PIGMENTOSA 62 | (OMIM:614181) |
Wagner disease | (Orphanet:898) |