Constriction of peripheral visual field
Symptom Information:
Symptom ID: | HPO:0001133 | |||||||||
Synonyms: |
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Quality: | ||||||||||
Cross references: |
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Is a (Direct Parents): | ||||||||||
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) Constriction of peripheral visual field(HPO:0001133) MedDRA: |
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Database Frequency: | 33 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
Alström syndrome | (Orphanet:64) |
Autosomal recessive optic atrophy, OPA7 type | (Orphanet:227976) |
Bietti crystalline dystrophy | (Orphanet:41751) |
CONE-ROD DYSTROPHY 20 | (OMIM:615973) |
Cherubism | (Orphanet:184) |
Choroideremia | (Orphanet:180) |
Choroideremia - deafness - obesity | (Orphanet:1435) |
Cone rod dystrophy | (Orphanet:1872) |
GLAUCOMA 1, OPEN ANGLE, M | (OMIM:610535) |
Leber congenital amaurosis 15 | (OMIM:613843) |
Leber congenital amaurosis 3 | (OMIM:604232) |
Mohr-Tranebjaerg syndrome | (Orphanet:52368) |
RETINITIS PIGMENTOSA | (OMIM:268000) |
RETINITIS PIGMENTOSA 1 | (OMIM:180100) |
RETINITIS PIGMENTOSA 13 | (OMIM:600059) |
RETINITIS PIGMENTOSA 19 | (OMIM:601718) |
RETINITIS PIGMENTOSA 2 | (OMIM:312600) |
RETINITIS PIGMENTOSA 25 | (OMIM:602772) |
RETINITIS PIGMENTOSA 26 | (OMIM:608380) |
RETINITIS PIGMENTOSA 28 | (OMIM:606068) |
RETINITIS PIGMENTOSA 38 | (OMIM:613862) |
RETINITIS PIGMENTOSA 44 | (OMIM:613769) |
RETINITIS PIGMENTOSA 46 | (OMIM:612572) |
RETINITIS PIGMENTOSA 6 | (OMIM:312612) |
RETINITIS PIGMENTOSA 66 | (OMIM:615233) |
RETINITIS PIGMENTOSA 69 | (OMIM:615780) |
RETINITIS PIGMENTOSA 7 | (OMIM:608133) |
RETINITIS PIGMENTOSA 9 | (OMIM:180104) |
Retinitis pigmentosa | (Orphanet:791) |
Retinitis pigmentosa 10 | (OMIM:180105) |
SCLEROSTEOSIS 1 | (OMIM:269500) |
SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND DEMENTIA | (OMIM:182830) |
Sclerosteosis | (Orphanet:3152) |