Undetectable electroretinogram
Symptom Information:
Symptom ID: | HPO:0000550 | |||||||||||
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) Undetectable electroretinogram(HPO:0000550) MedDRA: |
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Database Frequency: | 25 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
ARIMA SYNDROME | (OMIM:243910) |
Bifunctional enzyme deficiency | (Orphanet:300) |
CLN1 disease | (Orphanet:228329) |
CLN2 disease | (Orphanet:228349) |
CLN3 disease | (Orphanet:228346) |
Goldmann-Favre syndrome | (Orphanet:53540) |
Joubert syndrome 22 | (OMIM:615665) |
Joubert syndrome with oculorenal defect | (Orphanet:2318) |
Late infantile neuronal ceroid lipofuscinosis | (Orphanet:168491) |
Leber congenital amaurosis 14 | (OMIM:613341) |
Leber congenital amaurosis 5 | (OMIM:604537) |
Leber congenital amaurosis 6 | (OMIM:613826) |
Leber congenital amaurosis 7 | (OMIM:613829) |
Leber congenital amaurosis 8 | (OMIM:613835) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 3 | (OMIM:253280) |
Posterior column ataxia - retinitis pigmentosa | (Orphanet:88628) |
Proximal tubulopathy - diabetes mellitus - cerebellar ataxia | (Orphanet:3390) |
RETINITIS PIGMENTOSA 25 | (OMIM:602772) |
RETINITIS PIGMENTOSA 27 | (OMIM:613750) |
RETINITIS PIGMENTOSA 36 | (OMIM:610599) |
RETINITIS PIGMENTOSA 41 | (OMIM:612095) |
RETINITIS PIGMENTOSA 69 | (OMIM:615780) |
Senior-Loken syndrome 3 | (OMIM:606995) |
USHER SYNDROME, TYPE I | (OMIM:276900) |
Usher syndrome type 1 | (Orphanet:231169) |