Mixed hearing impairment

Symptom Information:

Symptom ID: HPO:0000410
Synonyms:
HEARING LOSS, MIXED [HPO:0000410]
Mixed hearing loss [HPO:0000410]
Hearing loss, mixed [OMIM:Hearing loss, mixed]
Mixed hearing loss [OMIM:Mixed hearing loss]
Hearing loss, mixed (in some patients) [OMIM:Hearing loss, mixed (in some patients)]
Mixed hearing loss (50% of patients) [OMIM:Mixed hearing loss (50% of patients)]
Quality:
Cross references:
OMIM: "Hearing loss, mixed" [OMIM:Hearing loss, mixed]
OMIM: "Mixed hearing loss" [OMIM:Mixed hearing loss]
OMIM: "Hearing loss, mixed (in some patients)" [OMIM:Hearing loss, mixed (in some patients)]
OMIM: "Mixed hearing loss (50% of patients)" [OMIM:Mixed hearing loss (50% of patients)]
Is a (Direct Parents):
HPO         Conductive hearing impairment
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:
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)