Profound sensorineural hearing impairment
Symptom Information:
Symptom ID: | HPO:0011476 | ||
Synonyms: |
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Quality: | |||
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) Profound sensorineural hearing impairment(HPO:0011476) Hearing abnormality(HPO:0000364) Hearing impairment(HPO:0000365) Sensorineural hearing impairment(HPO:0000407) Profound sensorineural hearing impairment(HPO:0011476) MedDRA: |
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Database Frequency: | 7 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal recessive deafness-onychodystrophy syndrome | (Orphanet:79500) |
DEAFNESS, AUTOSOMAL RECESSIVE 24 | (OMIM:611022) |
DEAFNESS, AUTOSOMAL RECESSIVE 3 | (OMIM:600316) |
DEAFNESS, AUTOSOMAL RECESSIVE 46 | (OMIM:609647) |
DEAFNESS, AUTOSOMAL RECESSIVE 48 | (OMIM:609439) |
Deafness with labyrinthine aplasia, microtia, and microdontia | (Orphanet:90024) |
Lethal ataxia with deafness and optic atrophy | (Orphanet:1187) |