Abnormal auditory evoked potentials
Symptom Information:
Symptom ID: | HPO:0006958 | ||||
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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: |
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Database Frequency: | 12 / 7739 | ||||
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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) |