Visual field defect

Symptom Information:

Symptom ID: HPO:0001123
Synonyms:
VISUAL FIELD DEFECTS [HPO:0001123]
Visual field defects [OMIM:Visual field defects]
Visual field defects (middle age) [OMIM:Visual field defects (middle age)]
Visual field defects (severe in some patients) [OMIM:Visual field defects (severe in some patients)]
Quality:
Cross references:
OMIM: "Visual field defects" [OMIM:Visual field defects]
OMIM: "Visual field defects (middle age)" [OMIM:Visual field defects (middle age)]
OMIM: "Visual field defects (severe in some patients)" [OMIM:Visual field defects (severe in some patients)]
Is a (Direct Parents):
HPO         Blind-spot enlargment
HPO         Abnormality of vision
HPO         Abnormal visual field test
HPO         Altitudinal visual field defect
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:
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)