Abnormal electroretinogram
Symptom Information:
Symptom ID: | HPO:0000512 | |||||||||||||||
Synonyms: |
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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) |
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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) |