Scotoma

Symptom Information:

Symptom ID: HPO:0000575
Synonyms:
Visual field scotoma (finding) [Orphanet:5810]
Visual field defect (finding) [Orphanet:5810]
Scotoma [Orphanet:5810]
Abnormal visual field/hemianopsia/hemianopia/scotoma/visual peripheral rim [Orphanet:5810]
Visual field defect [Orphanet:5810]
Visual field defect [MedDRA:10047555]
Defect visual field (NOS) [MedDRA:10047555]
Generalized visual field contraction or constriction [MedDRA:10047555]
Mariotte's spot enlarged [MedDRA:10047555]
Other localized visual field defect [MedDRA:10047555]
Peripheral vision defective [MedDRA:10047555]
Sector or arcuate visual field defects [MedDRA:10047555]
Vision peripheral decreased [MedDRA:10047555]
Vision peripheral defective [MedDRA:10047555]
Visual field constriction [MedDRA:10047555]
Visual field defect NOS [MedDRA:10047555]
Visual field defect, unspecified [MedDRA:10047555]
Visual field defects [MedDRA:10047555]
Scotoma [MedDRA:10039729]
Arcuate scotoma [MedDRA:10039729]
Blind spot enlarged [MedDRA:10039729]
Central scotoma [MedDRA:10039729]
Scotoma annular [MedDRA:10039729]
Scotoma central [MedDRA:10039729]
Scotoma involving central area [MedDRA:10039729]
Scotoma of blind spot area [MedDRA:10039729]
Scotoma peripheral [MedDRA:10039729]
Scotoma transient [MedDRA:10039729]
Vision central defective [MedDRA:10039729]
Central scotoma (in some patients) [OMIM:Central scotoma (in some patients)]
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:
Orphanet:5810 "Abnormal visual field/hemianopsia/hemianopia/scotoma/visual peripheral rim" [Orphanet:5810]
OMIM: "Central scotoma (in some patients)" [OMIM:Central scotoma (in some patients)]
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)]
UMLS:C0036454 "Scotoma" [Orphanet:5810]
Is a (Direct Parents):
MedDRA Visual field disorders
Orphanet Abnormality of the eye
HPO         Paracentral scotoma
HPO         Arcuate scotoma
HPO         Visual field defect
HPO         Ring scotoma
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)
MedDRA:
Eye disorders(MedDRA:10015919)
    Vision disorders(MedDRA:10047518)
       Visual field disorders(MedDRA:10047559)
          Scotoma(HPO:0000575)
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive spastic paraplegia type 55 (Orphanet:320375)
Bietti crystalline dystrophy (Orphanet:41751)
Cone dystrophy with supernormal rod response (Orphanet:209932)
Familial vascular leukoencephalopathy (Orphanet:36383)
Late-onset retinal degeneration (Orphanet:67042)
MELAS (Orphanet:550)
NEWFOUNDLAND ROD-CONE DYSTROPHY (OMIM:607476)
Posterior column ataxia - retinitis pigmentosa (Orphanet:88628)
RETINITIS PIGMENTOSA 18 (OMIM:601414)
RETINITIS PIGMENTOSA 62 (OMIM:614181)
Wagner disease (Orphanet:898)