Constriction of peripheral visual field

Symptom Information:

Symptom ID: HPO:0001133
Synonyms:
Depressed visual field [HPO:0001133]
Reduced visual fields [HPO:0001133]
Visual field constriction [HPO:0001133]
Constricted visual fields [OMIM:Constricted visual fields]
Depressed visual field [OMIM:Depressed visual field]
Reduced visual fields [OMIM:Reduced visual fields]
Visual field constriction [OMIM:Visual field constriction]
Constricted visual fields (occurs second) [OMIM:Constricted visual fields (occurs second)]
Visual fields reduced [OMIM:Visual fields reduced]
Quality:
Cross references:
OMIM: "Constricted visual fields" [OMIM:Constricted visual fields]
OMIM: "Depressed visual field" [OMIM:Depressed visual field]
OMIM: "Reduced visual fields" [OMIM:Reduced visual fields]
OMIM: "Visual field constriction" [OMIM:Visual field constriction]
OMIM: "Constricted visual fields (occurs second)" [OMIM:Constricted visual fields (occurs second)]
OMIM: "Visual fields reduced" [OMIM:Visual fields reduced]
Is a (Direct Parents):
HPO         Peripheral visual field constriction with 20-30 degrees central field preserved
HPO         Peripheral visual field constriction with 40-50 degrees central field preserved
HPO         Visual field defect
HPO         Peripheral visual field constriction with >50 degrees central field preserved
HPO         Peripheral visual field constriction with 30-40 degrees central field preserved
HPO         Peripheral visual field constriction with <10 degrees central field preserved
HPO         Peripheral visual field constriction with 10-20 degrees central field preserved
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:
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)