Bilateral sensorineural hearing impairment

Symptom Information:

Symptom ID: HPO:0008619
Synonyms:
Bilateral nerve deafness [HPO:0008619]
Bilateral sensorineural deafness [HPO:0008619]
Bilateral sensorineural hearing loss [HPO:0008619]
Hearing loss, sensorineural, bilateral [HPO:0008619]
Bilateral sensorineural deafness [OMIM:Bilateral sensorineural deafness]
Hearing loss, sensorineural, bilateral [OMIM:Hearing loss, sensorineural, bilateral]
Bilateral sensorineural hearing loss (in some patients) [OMIM:Bilateral sensorineural hearing loss (in some patients)]
Hearing loss, bilateral sensorineural (profound) [OMIM:Hearing loss, bilateral sensorineural (profound)]
Quality:
Cross references:
OMIM: "Bilateral sensorineural deafness" [OMIM:Bilateral sensorineural deafness]
OMIM: "Hearing loss, sensorineural, bilateral" [OMIM:Hearing loss, sensorineural, bilateral]
OMIM: "Bilateral sensorineural hearing loss (in some patients)" [OMIM:Bilateral sensorineural hearing loss (in some patients)]
OMIM: "Hearing loss, bilateral sensorineural (profound)" [OMIM:Hearing loss, bilateral sensorineural (profound)]
Is a (Direct Parents):
HPO         Sensorineural 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)
                Sensorineural hearing impairment(HPO:0000407)
                   Bilateral sensorineural hearing impairment(HPO:0008619)
          Abnormality of the inner ear(HPO:0000359)
             Functional abnormality of the inner ear(HPO:0011389)
                Sensorineural hearing impairment(HPO:0000407)
                   Bilateral sensorineural hearing impairment(HPO:0008619)
MedDRA:
Database Frequency: 23 / 7739
Resource:

All diseases associated with this symptom:

17q12 microdeletion syndrome (Orphanet:261265)
Autosomal recessive deafness-onychodystrophy syndrome (Orphanet:79500)
Autosomal recessive distal renal tubular acidosis without deafness (Orphanet:93609)
Connective tissue disorder due to lysyl hydroxylase-3 deficiency (Orphanet:300284)
DEAFNESS, AUTOSOMAL DOMINANT 11 (OMIM:601317)
DEAFNESS, AUTOSOMAL DOMINANT 20 (OMIM:604717)
DEAFNESS, AUTOSOMAL DOMINANT 39, WITH DENTINOGENESIS IMPERFECTA 1 (OMIM:605594)
DEAFNESS, AUTOSOMAL RECESSIVE 101 (OMIM:615837)
DEAFNESS, SENSORINEURAL, WITH PERIPHERAL NEUROPATHY AND ARTERIAL DISEASE (OMIM:124950)
Deafness, autosomal dominant 41 (OMIM:608224)
Deafness-infertility syndrome (Orphanet:94064)
EPSTEIN SYNDROME (OMIM:153650)
Jervell and Lange-Nielsen syndrome (Orphanet:90647)
Lethal ataxia with deafness and optic atrophy (Orphanet:1187)
MELAS (Orphanet:550)
Peroxisomal acyl-CoA oxidase deficiency (Orphanet:2971)
Perrault Syndrome 5 (OMIM:616138)
Reticular dysgenesis (Orphanet:33355)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)
Spastic paraplegia - nephritis - deafness (Orphanet:2820)
Temtamy preaxial brachydactyly syndrome (Orphanet:363417)
Tietz syndrome (Orphanet:42665)
X-linked Charcot-Marie-Tooth disease type 5 (Orphanet:99014)