Undetectable electroretinogram

Symptom Information:

Symptom ID: HPO:0000550
Synonyms:
Abolished electroretinogram [HPO:0000550]
Absent electroretinogram [HPO:0000550]
Extinction of electroretinogram [HPO:0000550]
Extinguished electroretinogram [HPO:0000550]
No light-evoked response on electroretinogram [HPO:0000550]
Abolished electroretinogram (ERG) [OMIM:Abolished electroretinogram (ERG)]
Absent electroretinogram [OMIM:Absent electroretinogram]
Extinguished electroretinogram [OMIM:Extinguished electroretinogram]
Abolished electroretinogram (ERG) (76%) [OMIM:Abolished electroretinogram (ERG) (76%)]
Extinction of electroretinogram (before age 10) [OMIM:Extinction of electroretinogram (before age 10)]
No light-evoked response on electroretinogram (ERG) [OMIM:No light-evoked response on electroretinogram (ERG)]
Quality:
Cross references:
OMIM: "Abolished electroretinogram (ERG)" [OMIM:Abolished electroretinogram (ERG)]
OMIM: "Absent electroretinogram" [OMIM:Absent electroretinogram]
OMIM: "Extinguished electroretinogram" [OMIM:Extinguished electroretinogram]
OMIM: "Abolished electroretinogram (ERG) (76%)" [OMIM:Abolished electroretinogram (ERG) (76%)]
OMIM: "Extinction of electroretinogram (before age 10)" [OMIM:Extinction of electroretinogram (before age 10)]
OMIM: "No light-evoked response on electroretinogram (ERG)" [OMIM:No light-evoked response on 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)
                            Undetectable electroretinogram(HPO:0000550)
MedDRA:
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)