Abnormal nervous system electrophysiology

Symptom Information:

Symptom ID: HPO:0001311
Synonyms:
Neurophysiologic abnormalities [HPO:0001311]
Neurophysiologic abnormalities (EEG, VEP, SEP) [HPO:0001311]
Neurophysiologic abnormalities (EEG, VEP, SEP) [OMIM:Neurophysiologic abnormalities (EEG, VEP, SEP)]
Neurophysiologic abnormalities (EEG, SEP, VEP) [OMIM:Neurophysiologic abnormalities (EEG, SEP, VEP)]
Quality:
Cross references:
OMIM: "Neurophysiologic abnormalities (EEG, VEP, SEP)" [OMIM:Neurophysiologic abnormalities (EEG, VEP, SEP)]
OMIM: "Neurophysiologic abnormalities (EEG, SEP, VEP)" [OMIM:Neurophysiologic abnormalities (EEG, SEP, VEP)]
Is a (Direct Parents):
HPO         Abnormality of peripheral nervous system electrophysiology
HPO         Abnormality of central nervous system electrophysiology
HPO         Abnormality of nervous system physiology
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system physiology(HPO:0012638)
             Abnormal nervous system electrophysiology(HPO:0001311)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

CLN2 disease (Orphanet:228349)
CLN5 disease (Orphanet:228360)
CLN6 disease (Orphanet:228363)
Late infantile neuronal ceroid lipofuscinosis (Orphanet:168491)