Abnormal auditory evoked potentials

Symptom Information:

Symptom ID: HPO:0006958
Synonyms:
Abnormal brainstem auditory-evoked potentials [HPO:0006958]
Abnormal auditory evoked potentials [OMIM:Abnormal auditory evoked potentials]
Abnormal brainstem auditory-evoked potentials [OMIM:Abnormal brainstem auditory-evoked potentials]
Abnormal brainstem auditory evoked potentials (BAEP) [OMIM:Abnormal brainstem auditory evoked potentials (BAEP)]
Quality:
Cross references:
OMIM: "Abnormal auditory evoked potentials" [OMIM:Abnormal auditory evoked potentials]
OMIM: "Abnormal brainstem auditory-evoked potentials" [OMIM:Abnormal brainstem auditory-evoked potentials]
OMIM: "Abnormal brainstem auditory evoked potentials (BAEP)" [OMIM:Abnormal brainstem auditory evoked potentials (BAEP)]
Is a (Direct Parents):
HPO         Abnormal nervous system electrophysiology
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)
                Abnormal auditory evoked potentials(HPO:0006958)
MedDRA:
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

ABCD SYNDROME (OMIM:600501)
AUDITORY NEUROPATHY, AUTOSOMAL DOMINANT, 1 (OMIM:609129)
AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVEFACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES (OMIM:109120)
Acrocraniofacial dysostosis (Orphanet:949)
Autosomal dominant optic atrophy and congenital deafness (Orphanet:3212)
COCKAYNE SYNDROME A (OMIM:216400)
COCKAYNE SYNDROME, TYPE III (OMIM:216411)
Charcot-Marie-Tooth disease type 4B1 (Orphanet:99955)
Charcot-Marie-Tooth disease type 4D (Orphanet:99950)
Cockayne syndrome (Orphanet:191)
Freeman-Sheldon syndrome (Orphanet:2053)
KRABBE DISEASE (OMIM:245200)