Visual field defect
Symptom Information:
Symptom ID: | HPO:0001123 | ||||||||
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) MedDRA: |
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Database Frequency: | 30 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT | (OMIM:206570) |
Adult-onset foveomacular vitelliform dystrophy | (Orphanet:99000) |
BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME | (OMIM:615722) |
Bardet-Biedl syndrome 1 | (OMIM:209900 ) |
Best vitelliform macular dystrophy | (Orphanet:1243) |
Biotinidase deficiency | (Orphanet:79241) |
Familial thrombocytosis | (Orphanet:71493) |
Friedreich ataxia 1 | (OMIM:229300) |
GLAUCOMA 1, OPEN ANGLE, P | (OMIM:177700) |
Isolated plagiocephaly | (Orphanet:35098) |
LEUKOENCEPHALOPATHY WITH ATAXIA | (OMIM:615651) |
MACULAR DYSTROPHY, VITELLIFORM, 1 | (OMIM:153840) |
MELAS | (Orphanet:550) |
NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1 | (OMIM:610445) |
Non-polyposis Turcot syndrome | (Orphanet:99817) |
PORENCEPHALY 1 | (OMIM:175780) |
Porencephaly | (Orphanet:2940) |
RETINITIS PIGMENTOSA 31 | (OMIM:609923) |
RETINITIS PIGMENTOSA 39 | (OMIM:613809) |
RETINITIS PIGMENTOSA 4 | (OMIM:613731) |
RETINITIS PIGMENTOSA 62 | (OMIM:614181) |
RETINITIS PIGMENTOSA 68 | (OMIM:615725) |
Retinitis pigmentosa 10 | (OMIM:180105) |
Rift valley fever | (Orphanet:319251) |
Sneddon syndrome | (Orphanet:820) |
Usher syndrome | (Orphanet:886) |
Usher syndrome type 1 | (Orphanet:231169) |
Usher syndrome type 2 | (Orphanet:231178) |
Usher syndrome type 3 | (Orphanet:231183) |
Wagner disease | (Orphanet:898) |