Decreased light- and dark-adapted electroretinogram amplitude

Symptom Information:

Symptom ID: HPO:0000654
Synonyms:
Decreased amplitudes on flash visual electroretinogram [HPO:0000654]
Decreased electroretinogram [HPO:0000654]
Decreased electroretinogram response [HPO:0000654]
Flattened or absent electroretinogram [HPO:0000654]
Reduced electroretinogram [HPO:0000654]
Reduced electroretinogram (ERG) [HPO:0000654]
Reduced or abolished electroretinogram [HPO:0000654]
Decreased amplitudes on flash visual electroretinogram [OMIM:Decreased amplitudes on flash visual electroretinogram]
Reduced electroretinogram (ERG) [OMIM:Reduced electroretinogram (ERG)]
Decreased electroretinogram (ERG) [OMIM:Decreased electroretinogram (ERG)]
Decreased electroretinogram (ERG) response [OMIM:Decreased electroretinogram (ERG) response]
Reduced or abolished electroretinogram (ERG) [OMIM:Reduced or abolished electroretinogram (ERG)]
Quality:
Cross references:
OMIM: "Decreased amplitudes on flash visual electroretinogram" [OMIM:Decreased amplitudes on flash visual electroretinogram]
OMIM: "Reduced electroretinogram (ERG)" [OMIM:Reduced electroretinogram (ERG)]
OMIM: "Decreased electroretinogram (ERG)" [OMIM:Decreased electroretinogram (ERG)]
OMIM: "Decreased electroretinogram (ERG) response" [OMIM:Decreased electroretinogram (ERG) response]
OMIM: "Reduced or abolished electroretinogram (ERG)" [OMIM:Reduced or abolished electroretinogram (ERG)]
Is a (Direct Parents):
HPO         Abnormal electroretinogram
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye morphology(HPO:0012372)
             Abnormality of the globe(HPO:0012374)
                Abnormality of the posterior segment of the globe(HPO:0004329)
                   Abnormality of the fundus(HPO:0001098)
                      Abnormality of the retina(HPO:0000479)
                         Abnormal electroretinogram(HPO:0000512)
                            Decreased light- and dark-adapted electroretinogram amplitude(HPO:0000654)
MedDRA:
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

ALG3-CDG (Orphanet:79321)
CLN1 disease (Orphanet:228329)
CLN9 disease (Orphanet:228357)
Leber congenital amaurosis 1 (OMIM:204000)
Leber congenital amaurosis 14 (OMIM:613341)
Leber congenital amaurosis 2 (OMIM:204100)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 3 (OMIM:253280)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 6 (OMIM:608840)
Mucolipidosis type 4 (Orphanet:578)
NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1 (OMIM:610445)
Peroxisomal acyl-CoA oxidase deficiency (Orphanet:2971)
RETINITIS PIGMENTOSA 44 (OMIM:613769)
RETINITIS PIGMENTOSA 46 (OMIM:612572)
RETINITIS PIGMENTOSA 47 (OMIM:613758)
Retinopathy, Burgess-Black type (Orphanet:139455)
STRIATONIGRAL DEGENERATION, INFANTILE, MITOCHONDRIAL (OMIM:500003)
X-linked cone dysfunction syndrome with myopia (Orphanet:90001)