Cochlear degeneration
Symptom Information:
Symptom ID: | HPO:0005102 | ||
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 ear(HPO:0000598) Abnormality of the inner ear(HPO:0000359) Morphological abnormality of the inner ear(HPO:0011390) Abnormality of cochlea(HPO:0000375) Cochlear degeneration(HPO:0005102) MedDRA: |
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Database Frequency: | 5 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal recessive cerebellar ataxia - blindness - deafness | (Orphanet:95433) |
DEAFNESS, AUTOSOMAL DOMINANT 9 | (OMIM:601369) |
MELAS | (Orphanet:550) |
OPTICOCOCHLEODENTATE DEGENERATION | (OMIM:258700) |
PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRALDYSFUNCTION | (OMIM:172500) |