High-frequency hearing impairment

Symptom Information:

Symptom ID: HPO:0005101
Synonyms:
Hearing loss, high-frequency [HPO:0005101]
High frequency hearing loss [HPO:0005101]
High-frequency deafness [HPO:0005101]
Progressive high frequency hearing loss [HPO:0005101]
Progressive high-frequency hearing loss [HPO:0005101]
Hearing loss, high-frequency (onset in childhood-adolescence) [OMIM:Hearing loss, high-frequency (onset in childhood-adolescence)]
High-frequency hearing loss [OMIM:High-frequency hearing loss]
Progressive high-frequency hearing loss (onset 20-30 years) [OMIM:Progressive high-frequency hearing loss (onset 20-30 years)]
Quality:
Cross references:
OMIM: "Hearing loss, high-frequency (onset in childhood-adolescence)" [OMIM:Hearing loss, high-frequency (onset in childhood-adolescence)]
OMIM: "High-frequency hearing loss" [OMIM:High-frequency hearing loss]
OMIM: "Progressive high-frequency hearing loss (onset 20-30 years)" [OMIM:Progressive high-frequency hearing loss (onset 20-30 years)]
Is a (Direct Parents):
HPO         Hearing impairment
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:
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)