Abnormal electroretinogram

Symptom Information:

Symptom ID: HPO:0000512
Synonyms:
Abnormal electroretinogram (ERG) [HPO:0000512]
Abnormal electroretinography [HPO:0000512]
Abnormal ERG [HPO:0000512]
ERG abnormal [HPO:0000512]
FLATTENED OR ABSENT ELECTRORETINOGRAM (ERG) [HPO:0000512]
Electroretinogram abnormal (finding) [Orphanet:5750]
Electroretinogram abnormal [Orphanet:5750]
Abnormal ERG [OMIM:Abnormal ERG]
Abnormal electroretinogram [OMIM:Abnormal electroretinogram]
Abnormal electroretinogram (ERG) [OMIM:Abnormal electroretinogram (ERG)]
Flattened or absent electroretinogram (ERG) [OMIM:Flattened or absent electroretinogram (ERG)]
Abnormal ERG/electroretinogram/electroretinography [Orphanet:5750]
Retinogram abnormal [MedDRA:10059663]
Electroretinogram abnormal [MedDRA:10059663]
Retinal photography abnormal [MedDRA:10059663]
Quality:
Cross references:
Orphanet:5750 "Abnormal ERG/electroretinogram/electroretinography" [Orphanet:5750]
OMIM: "Abnormal ERG" [OMIM:Abnormal ERG]
OMIM: "Abnormal electroretinogram" [OMIM:Abnormal electroretinogram]
OMIM: "Abnormal electroretinogram (ERG)" [OMIM:Abnormal electroretinogram (ERG)]
OMIM: "Flattened or absent electroretinogram (ERG)" [OMIM:Flattened or absent electroretinogram (ERG)]
UMLS:C0476397 "Electroretinogram abnormal" [Orphanet:5750]
Is a (Direct Parents):
Orphanet Abnormality of the eye
MedDRA Ophthalmic histopathology and imaging procedures
HPO         Abnormality of the retina
HPO         Abnormal pattern electroretinogram
HPO         Abnormal full-field electroretinogram
HPO         Abnormal multifocal 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)
MedDRA:
Investigations(MedDRA:10022891)
    Neurological, special senses and psychiatric investigations(MedDRA:10029295)
       Ophthalmic histopathology and imaging procedures(MedDRA:10030866)
          Abnormal electroretinogram(HPO:0000512)
Database Frequency: 61 / 7739
Resource:

All diseases associated with this symptom:

AICA-ribosiduria (Orphanet:250977)
Arthrogryposis with oculomotor limitation and electroretinal anomalies (Orphanet:1154)
Autosomal dominant neovascular inflammatory vitreoretinopathy (Orphanet:329211)
Autosomal dominant vitreoretinochoroidopathy (Orphanet:3086)
Bardet-Biedl syndrome (Orphanet:110)
Best vitelliform macular dystrophy (Orphanet:1243)
Blue cone monochromatism (Orphanet:16)
Bothnia retinal dystrophy (Orphanet:85128)
CADASIL (Orphanet:136)
CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME (OMIM:614195)
Cerebellar ataxia - areflexia - pes cavus - optic atrophy - sensorineural hearing loss (Orphanet:1171)
Cerebellar ataxia - hypogonadism (Orphanet:1173)
Cerebellar hypoplasia - tapetoretinal degeneration (Orphanet:2246)
Choroideremia (Orphanet:180)
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome (Orphanet:1369)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28 (OMIM:616211)
Ectopia lentis - chorioretinal dystrophy - myopia (Orphanet:1884)
Glycogen storage disease due to LAMP-2 deficiency (Orphanet:34587)
Infantile neuronal ceroid lipofuscinosis (Orphanet:79263)
Joubert syndrome 3 (OMIM:608629)
Joubert syndrome with ocular defect (Orphanet:220493)
Juvenile neuronal ceroid lipofuscinosis (Orphanet:79264)
Late infantile neuronal ceroid lipofuscinosis (Orphanet:168491)
Leber congenital amaurosis (Orphanet:65)
Leber hereditary optic neuropathy (Orphanet:104)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria (Orphanet:1933)
Mohr-Tranebjaerg syndrome (Orphanet:52368)
Mucolipidosis type 4 (Orphanet:578)
Multiple non-ossifying fibromatosis (Orphanet:2029)
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C (OMIM:613216)
Nephronophthisis 15 (OMIM:614845)
Neuronal ceroid lipofuscinosis (Orphanet:216)
Night blindness - skeletal anomalies - dysmorphism (Orphanet:1390)
OPTIC ATROPHY WITH NEGATIVE ELECTRORETINOGRAMS (OMIM:165510)
Oligocone trichromacy (Orphanet:75378)
Ophthalmoplegia - intellectual deficit - lingua scrotalis (Orphanet:2743)
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) (OMIM:214100)
PEROXISOME BIOGENESIS DISORDER 3B (OMIM:266510)
Peroxisomal acyl-CoA oxidase deficiency (Orphanet:2971)
Progressive cone dystrophy (Orphanet:1871)
Proximal tubulopathy - diabetes mellitus - cerebellar ataxia (Orphanet:3390)
RETINITIS PIGMENTOSA 19 (OMIM:601718)
RETINITIS PIGMENTOSA 31 (OMIM:609923)
RETINITIS PIGMENTOSA 39 (OMIM:613809)
RETINITIS PIGMENTOSA 4 (OMIM:613731)
RETINITIS PIGMENTOSA 43 (OMIM:613810)
RETINITIS PIGMENTOSA 50 (OMIM:613194)
RETINITIS PIGMENTOSA 54 (OMIM:613428)
RETINITIS PIGMENTOSA 7 (OMIM:608133)
RETINOSCHISIS OF FOVEA (OMIM:268080)
Retinal degeneration - nanophthalmos - glaucoma (Orphanet:1574)
Retinitis pigmentosa (Orphanet:791)
Ruvalcaba syndrome (Orphanet:3121)
Usher syndrome (Orphanet:886)
Usher syndrome type 1 (Orphanet:231169)
Usher syndrome type 2 (Orphanet:231178)
Usher syndrome type 3 (Orphanet:231183)
Van den Bosch syndrome (Orphanet:3417)
X-linked retinoschisis (Orphanet:792)
Zellweger syndrome (Orphanet:912)
Zellweger-like syndrome without peroxisomal anomalies (Orphanet:50812)