Progressive hearing impairment

Symptom Information:

Symptom ID: HPO:0001730
Synonyms:
Progressive hearing loss [HPO:0001730]
Progressive hearing loss [OMIM:Progressive hearing loss]
Hearing loss, progressive [OMIM:Hearing loss, progressive]
Hearing loss, progressive (in some patients) [OMIM:Hearing loss, progressive (in some patients)]
Progressive hearing loss (in some) [OMIM:Progressive hearing loss (in some)]
Quality:
Cross references:
OMIM: "Progressive hearing loss" [OMIM:Progressive hearing loss]
OMIM: "Hearing loss, progressive" [OMIM:Hearing loss, progressive]
OMIM: "Hearing loss, progressive (in some patients)" [OMIM:Hearing loss, progressive (in some patients)]
OMIM: "Progressive hearing loss (in some)" [OMIM:Progressive hearing loss (in some)]
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)
                Progressive hearing impairment(HPO:0001730)
MedDRA:
Database Frequency: 29 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant nonsyndromic sensorineural deafness type DFNA (Orphanet:90635)
CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT (OMIM:122860)
DEAFNESS WITH ANHIDROTIC ECTODERMAL DYSPLASIA (OMIM:125050)
DEAFNESS, AUTOSOMAL DOMINANT 1 (OMIM:124900)
DEAFNESS, AUTOSOMAL DOMINANT 18 (OMIM:606012)
DEAFNESS, AUTOSOMAL DOMINANT 49 (OMIM:608372)
DEAFNESS, AUTOSOMAL DOMINANT 50 (OMIM:613074)
DEAFNESS, AUTOSOMAL DOMINANT 65 (OMIM:616044)
DEAFNESS, AUTOSOMAL RECESSIVE 30 (OMIM:607101)
DEAFNESS, AUTOSOMAL RECESSIVE 91 (OMIM:613453)
DEAFNESS, MID-TONE NEURAL (OMIM:124700)
DEAFNESS, SENSORINEURAL, WITH PERIPHERAL NEUROPATHY AND ARTERIAL DISEASE (OMIM:124950)
Deafness, autosomal dominant 41 (OMIM:608224)
Hurler syndrome (Orphanet:93473)
Mohr-Tranebjaerg syndrome (Orphanet:52368)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 2, severe form (Orphanet:217085)
PEROXISOME BIOGENESIS DISORDER 14B (OMIM:614920)
POLYENDOCRINE-POLYNEUROPATHY SYNDROME (OMIM:616113)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3 (OMIM:609286)
Perrault Syndrome 3 (OMIM:614129)
Perrault Syndrome 4 (OMIM:615300)
Perrault Syndrome 5 (OMIM:616138)
Scheie syndrome (Orphanet:93474)
Spinocerebellar ataxia type 36 (Orphanet:276198)
VESTIBULOCOCHLEAR DYSFUNCTION, PROGRESSIVE (OMIM:193005)
Wolfram syndrome 1 (OMIM:222300)
Wolfram-like syndrome (ORPHA:411590)
X-linked hereditary sensory and autonomic neuropathy with deafness (Orphanet:139583)