Profound sensorineural hearing impairment

Symptom Information:

Symptom ID: HPO:0011476
Synonyms:
Quality:
Cross references:
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)
          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:
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)