High-frequency hearing impairment
Symptom Information:
Symptom ID: | HPO:0005101 | ||||||||
Synonyms: |
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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) Hearing abnormality(HPO:0000364) Hearing impairment(HPO:0000365) High-frequency hearing impairment(HPO:0005101) MedDRA: |
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Database Frequency: | 16 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
Alström syndrome | (Orphanet:64) |
DEAFNESS, AUTOSOMAL DOMINANT 17 | (OMIM:603622) |
DEAFNESS, AUTOSOMAL DOMINANT 2B | (OMIM:612644) |
DEAFNESS, AUTOSOMAL DOMINANT 39, WITH DENTINOGENESIS IMPERFECTA 1 | (OMIM:605594) |
DEAFNESS, AUTOSOMAL DOMINANT 7 | (OMIM:601412) |
DEAFNESS, X-LINKED 4 | (OMIM:300066) |
Dyschromatosis universalis hereditaria 1 | (OMIM:127500) |
Dyschromatosis universalis hereditaria 2 | (OMIM:612715) |
Dyschromatosis universalis hereditaris 3 | (OMIM:615402) |
Fabry disease | (Orphanet:324) |
Intellectual deficit, X-linked - Dandy-Walker malformation - basal ganglia disease - Seizures | (Orphanet:1568) |
Perrault Syndrome 4 | (OMIM:615300) |
Primary ciliary dyskinesia - retinitis pigmentosa | (Orphanet:247522) |
Progeria - short stature - pigmented nevi | (Orphanet:2959) |
Wolfram syndrome 1 | (OMIM:222300) |
Wolfram syndrome 2 | (OMIM:604928) |