Mixed hearing impairment
Symptom Information:
Symptom ID: | HPO:0000410 | ||||||
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 middle ear(HPO:0000370) Functional abnormality of the middle ear(HPO:0011452) Conductive hearing impairment(HPO:0000405) Mixed hearing impairment(HPO:0000410) Hearing abnormality(HPO:0000364) Hearing impairment(HPO:0000365) Conductive hearing impairment(HPO:0000405) Mixed hearing impairment(HPO:0000410) MedDRA: |
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Database Frequency: | 22 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Acro-fronto-facio-nasal dysostosis | (Orphanet:1784) |
BOR syndrome | (Orphanet:107) |
BRACHYDACTYLY, TYPE A1, WITH SHORT STATURE, SCOLIOSIS, MICROCEPHALY,PTOSIS, HEARING LOSS, AND MENTAL RETARDATION | (OMIM:613627) |
BRANCHIOOTIC SYNDROME 1 | (OMIM:602588) |
BRANCHIOOTORENAL SYNDROME 1 | (OMIM:113650) |
Bilateral microtia - deafness - cleft palate | (Orphanet:140963) |
Branchiogenic deafness syndrome | (Orphanet:50815) |
CHARGE syndrome | (Orphanet:138) |
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT | (OMIM:123000) |
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE | (OMIM:218400) |
Craniometaphyseal dysplasia | (Orphanet:1522) |
Focal dermal hypoplasia | (Orphanet:2092) |
Hypospadias - hypertelorism - coloboma and deafness | (Orphanet:157788) |
Isolated Klippel-Feil syndrome | (Orphanet:2345) |
Lacrimo-auriculo-dento-digital syndrome | (Orphanet:2363) |
Lethal osteosclerotic bone dysplasia | (Orphanet:1832) |
MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA | (OMIM:608624) |
OTOFACIOCERVICAL SYNDROME 2 | (OMIM:615560) |
OTOSCLEROSIS 4 | (OMIM:611571) |
Otospondylomegaepiphyseal dysplasia | (Orphanet:1427) |
Spondylocarpotarsal synostosis | (Orphanet:3275) |
Timothy syndrome | (Orphanet:65283) |