Bilateral sensorineural hearing impairment
Symptom Information:
Symptom ID: | HPO:0008619 | ||||||||
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) 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) Hearing abnormality(HPO:0000364) Hearing impairment(HPO:0000365) Sensorineural hearing impairment(HPO:0000407) Bilateral sensorineural hearing impairment(HPO:0008619) MedDRA: |
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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) |