Progressive sensorineural hearing impairment
Symptom Information:
Symptom ID: | HPO:0000408 | ||||||||||||||||
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) Progressive sensorineural hearing impairment(HPO:0000408) Hearing abnormality(HPO:0000364) Hearing impairment(HPO:0000365) Progressive hearing impairment(HPO:0001730) Progressive sensorineural hearing impairment(HPO:0000408) Sensorineural hearing impairment(HPO:0000407) Progressive sensorineural hearing impairment(HPO:0000408) MedDRA: |
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Database Frequency: | 28 / 7739 | ||||||||||||||||
Resource: |
All diseases associated with this symptom:
Alström syndrome | (Orphanet:64) |
Ataxia-deafness-retardation syndrome | (Orphanet:1188) |
Autosomal dominant Charcot-Marie-Tooth disease type 2J | (Orphanet:99943) |
Autosomal dominant optic atrophy and congenital deafness | (Orphanet:3212) |
Autosomal dominant optic atrophy plus syndrome | (Orphanet:1215) |
CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURALHEARING LOSS | (OMIM:601338) |
Choroideremia - deafness - obesity | (Orphanet:1435) |
DEAFNESS, AUTOSOMAL DOMINANT 20 | (OMIM:604717) |
DEAFNESS, AUTOSOMAL DOMINANT 4A | (OMIM:600652) |
DEAFNESS, AUTOSOMAL DOMINANT 5 | (OMIM:600994) |
DEAFNESS, AUTOSOMAL DOMINANT 6 | (OMIM:600965) |
DEAFNESS, AUTOSOMAL RECESSIVE 76 | (OMIM:615540) |
DEAFNESS, AUTOSOMAL RECESSIVE 84A | (OMIM:613391) |
DEAFNESS, SENSORINEURAL, AUTOSOMAL-MITOCHONDRIAL TYPE | (OMIM:221745) |
Deafness, autosomal dominant 41 | (OMIM:608224) |
Fabry disease | (Orphanet:324) |
Flynn-Aird syndrome | (Orphanet:2047) |
Gingival fibromatosis - progressive deafness | (Orphanet:2027) |
MELAS | (Orphanet:550) |
MYH9-related thrombocytopenia | (Orphanet:182050) |
Maternally-inherited cardiomyopathy and hearing loss | (Orphanet:1349) |
Mitochondrial nonsyndromic sensorineural deafness | (Orphanet:90641) |
Mohr-Tranebjaerg syndrome | (Orphanet:52368) |
Muckle-Wells syndrome | (Orphanet:575) |
OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE | (OMIM:258650) |
PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRALDYSFUNCTION | (OMIM:172500) |
Wolfram-like syndrome | (ORPHA:411590) |
X-linked mixed deafness with perilymphatic gusher | (Orphanet:383) |