Central scotoma
Symptom Information:
Symptom ID: | HPO:0000603 | ||||
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) Central scotoma(HPO:0000603) MedDRA: |
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Database Frequency: | 18 / 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) |
Autosomal recessive optic atrophy, OPA7 type | (Orphanet:227976) |
Autosomal recessive spastic paraplegia type 55 | (Orphanet:320375) |
CONE-ROD DYSTROPHY 17 | (OMIM:615163) |
CONE-ROD DYSTROPHY 18 | (OMIM:615374) |
CONE-ROD DYSTROPHY 3 | (OMIM:604116) |
CONE-ROD DYSTROPHY, X-LINKED, 3 | (OMIM:300476) |
Hereditary motor and sensory neuropathy type 6 | (Orphanet:90120) |
Leber hereditary optic neuropathy | (Orphanet:104) |
MACULAR DYSTROPHY, VITELLIFORM, 5 | (OMIM:616152) |
Mohr-Tranebjaerg syndrome | (Orphanet:52368) |
Necrotizing encephalomyelopathy, subacute, of Leigh, adult | (OMIM:161700) |
OPTIC ATROPHY 1 | (OMIM:165500) |
OPTIC ATROPHY 5 | (OMIM:610708) |
RETINITIS PIGMENTOSA 66 | (OMIM:615233) |
Retinal macular dystrophy type 2 | (Orphanet:319640) |
[DEL] LEBER OPTIC ATROPHY | (OMIM:535000) |