Decreased light- and dark-adapted electroretinogram amplitude
Symptom Information:
Symptom ID: | HPO:0000654 | ||||||||||||
Synonyms: |
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Quality: | |||||||||||||
Cross references: |
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Is a (Direct Parents): |
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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) Decreased light- and dark-adapted electroretinogram amplitude(HPO:0000654) MedDRA: |
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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) |