Conductive hearing impairment

Symptom Information:

Symptom ID: HPO:0000405
Synonyms:
Conduction deafness [HPO:0000405]
Conductive deafness [HPO:0000405]
Conductive hearing loss [HPO:0000405]
Hearing loss, conductive [HPO:0000405]
Conductive hearing loss [Orphanet:13680]
Conductive hearing loss (disorder) [Orphanet:13680]
Conduction deafness [OMIM:Conduction deafness]
Conductive deafness [OMIM:Conductive deafness]
Conductive hearing loss [OMIM:Conductive hearing loss]
Hearing loss, conductive [OMIM:Hearing loss, conductive]
Conductive deafness/hearing loss [Orphanet:13680]
Conductive deafness [Orphanet:13680]
Conductive deafness [MedDRA:10010280]
Conductive deafness (excl otosclerosis) [MedDRA:10010280]
Conductive hearing loss [MedDRA:10010280]
Conductive hearing loss of combined types [MedDRA:10010280]
Conductive hearing loss, external ear [MedDRA:10010280]
Conductive hearing loss, inner ear [MedDRA:10010280]
Conductive hearing loss, middle ear [MedDRA:10010280]
Conductive hearing loss, tympanic membrane [MedDRA:10010280]
Conductive hearing loss, unspecified [MedDRA:10010280]
Deafness conductive (excl otosclerosis) [MedDRA:10010280]
Deafness middle ear [MedDRA:10010280]
Deafness middle ear type [MedDRA:10010280]
Deafness partial conductive (excl otosclerosis) [MedDRA:10010280]
Partial conductive deafness [MedDRA:10010280]
Conductive hearing loss (30% of patients) [OMIM:Conductive hearing loss (30% of patients)]
Conductive hearing loss (in a subset of patients) [OMIM:Conductive hearing loss (in a subset of patients)]
Deafness, conductive [OMIM:Deafness, conductive]
Deafness, conductive (in some patients) [OMIM:Deafness, conductive (in some patients)]
Hearing loss, conductive (in some patients) [OMIM:Hearing loss, conductive (in some patients)]
Hearing loss, conductive (rare) [OMIM:Hearing loss, conductive (rare)]
Quality:
Cross references:
HPO:0008513 "Bilateral conductive hearing impairment" [Orphanet:13680]
HPO:0008591 "Congenital conductive hearing impairment" [Orphanet:13680]
Orphanet:13680 "Conductive deafness/hearing loss" [Orphanet:13680]
OMIM: "Conduction deafness" [OMIM:Conduction deafness]
OMIM: "Conductive deafness" [OMIM:Conductive deafness]
OMIM: "Conductive hearing loss" [OMIM:Conductive hearing loss]
OMIM: "Hearing loss, conductive" [OMIM:Hearing loss, conductive]
OMIM: "Conductive hearing loss (30% of patients)" [OMIM:Conductive hearing loss (30% of patients)]
OMIM: "Conductive hearing loss (in a subset of patients)" [OMIM:Conductive hearing loss (in a subset of patients)]
OMIM: "Deafness, conductive" [OMIM:Deafness, conductive]
OMIM: "Deafness, conductive (in some patients)" [OMIM:Deafness, conductive (in some patients)]
OMIM: "Hearing loss, conductive (in some patients)" [OMIM:Hearing loss, conductive (in some patients)]
OMIM: "Hearing loss, conductive (rare)" [OMIM:Hearing loss, conductive (rare)]
UMLS:C0018777 "Conductive hearing loss" [Orphanet:13680]
Is a (Direct Parents):
HPO         Moderate conductive hearing impairment
HPO         Severe conductive hearing impairment
HPO         Hearing impairment
HPO         Unilateral conductive hearing impairment
HPO         Functional abnormality of the middle ear
Orphanet Hearing impairment
MedDRA Hearing impairment
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the ear(HPO:0000598)
          Hearing abnormality(HPO:0000364)
             Hearing impairment(HPO:0000365)
                Conductive hearing impairment(HPO:0000405)
          Abnormality of the middle ear(HPO:0000370)
             Functional abnormality of the middle ear(HPO:0011452)
                Conductive hearing impairment(HPO:0000405)
MedDRA:
Ear and labyrinth disorders(MedDRA:10013993)
    Hearing disorders(MedDRA:10019243)
       Hearing impairment(HPO:0000365)
          Conductive hearing impairment(HPO:0000405)
Congenital, familial and genetic disorders(MedDRA:10010331)
    Ear and labyrinthine disorders congenital(MedDRA:10013995)
       Hearing disorders congenital(MedDRA:10019244)
          Hearing impairment(HPO:0000365)
             Conductive hearing impairment(HPO:0000405)
Database Frequency: 164 / 7739
Resource:

All diseases associated with this symptom:

19p13.12 microdeletion syndrome (Orphanet:254346)
1p36 deletion syndrome (Orphanet:1606)
2q37 microdeletion syndrome (Orphanet:1001)
3MC SYNDROME 1 (OMIM:257920)
ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS (OMIM:201750)
AURAL ATRESIA, CONGENITAL (OMIM:607842)
Abruzzo-Erickson syndrome (Orphanet:921)
Achondroplasia (Orphanet:15)
Acro-oto-ocular syndrome (Orphanet:2980)
Acro-renal-ocular syndrome (Orphanet:959)
Acrocraniofacial dysostosis (Orphanet:949)
Agenesis of the corpus callosum - intellectual deficit - coloboma - micrognathia (Orphanet:52055)
Agnathia - holoprosencephaly - situs inversus (Orphanet:990)
Alopecia antibody deficiency (Orphanet:1006)
Alström syndrome (Orphanet:64)
Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Apert syndrome (Orphanet:87)
Arterial calcification, generalized, of infancy, 1 (OMIM:208000)
Autosomal dominant Larsen syndrome (Orphanet:503)
Autosomal dominant Opitz G/BBB syndrome (Orphanet:306588)
Autosomal dominant osteopetrosis type 1 (Orphanet:2783)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
BRANCHIOOTIC SYNDROME 1 (OMIM:602588)
BRANCHIOOTORENAL SYNDROME 1 (OMIM:113650)
Baller-Gerold syndrome (Orphanet:1225)
Bardet-Biedl syndrome 16 (OMIM:615993)
Blepharo-cheilo-odontic syndrome (Orphanet:1997)
Blepharophimosis-intellectual deficit syndrome, Ohdo type (Orphanet:2728)
Branchio-oculo-facial syndrome (Orphanet:1297)
Branchio-otic syndrome (Orphanet:52429)
Branchiogenic deafness syndrome (Orphanet:50815)
Brittle cornea syndrome (Orphanet:90354)
CARPENTER SYNDROME 1 (OMIM:201000)
CILIARY DYSKINESIA, PRIMARY, 1 (OMIM:244400)
Cardiospondylocarpofacial syndrome (Orphanet:3238)
Carpenter syndrome (Orphanet:65759)
Caudal appendage - deafness (Orphanet:1123)
Cerebro-costo-mandibular syndrome (Orphanet:1393)
Cerebro-facio-articular syndrome (Orphanet:314679)
Choanal atresia - deafness - cardiac defects - dysmorphism (Orphanet:1200)
Choroideremia - deafness - obesity (Orphanet:1435)
Cleft palate - stapes fixation - oligodontia (Orphanet:2010)
Conductive deafness - malformed external ear (Orphanet:3216)
Conductive deafness - ptosis - skeletal anomalies (Orphanet:3236)
Cooper-Jabs syndrome (Orphanet:1488)
Cornelia de Lange syndrome (Orphanet:199)
Craniodiaphyseal dysplasia (Orphanet:1513)
Craniometaphyseal dysplasia (Orphanet:1522)
Crouzon disease (Orphanet:207)
Crouzon syndrome - acanthosis nigricans (Orphanet:93262)
DEAFNESS, AUTOSOMAL DOMINANT 23 (OMIM:605192)
DEAFNESS, CONDUCTIVE, WITH MALFORMED EXTERNAL EAR (OMIM:221300)
DIAMOND-BLACKFAN ANEMIA 10 (OMIM:613309)
DIAMOND-BLACKFAN ANEMIA 14 WITH MANDIBULOFACIAL DYSOSTOSIS (OMIM:300946)
Deafness - ear malformation - facial palsy (Orphanet:3232)
Distal limb deficiencies - micrognathia syndrome (Orphanet:1307)
Distal monosomy 19p13.3 (Orphanet:96129)
Down syndrome (Orphanet:870)
Dysmorphism - short stature - deafness - disorder of sex development (Orphanet:2282)
EEC syndrome (Orphanet:1896)
Ectodermal dysplasia syndrome (Orphanet:79373)
External auditory canal aplasia/hypoplasia (Orphanet:141074)
Familial expansile osteolysis (Orphanet:85195)
Fibrodysplasia ossificans progressiva (Orphanet:337)
Floating-Harbor syndrome (Orphanet:2044)
Fraser syndrome (Orphanet:2052)
Frontometaphyseal dysplasia (Orphanet:1826)
Frontonasal dysplasia (Orphanet:250)
Fucosidosis (Orphanet:349)
Giant cell arteritis (Orphanet:397)
Goldenhar syndrome (Orphanet:374)
Gorlin syndrome (Orphanet:377)
Gorlin-Chaudhry-Moss syndrome (Orphanet:2095)
HAJDU-CHENEY SYNDROME (OMIM:102500)
HUNTER-MACDONALD SYNDROME (OMIM:611962)
Hennekam syndrome (Orphanet:2136)
Hennekam-Beemer syndrome (Orphanet:2135)
High myopia-sensorineural deafness syndrome (Orphanet:363396)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hypertelorism-microtia-facial clefting syndrome (Orphanet:2213)
IMMUNODEFICIENCY 23 (OMIM:615816)
Intellectual deficit - cataracts - calcified pinnae - myopathy (Orphanet:3042)
Intellectual deficit - polydactyly - uncombable hair (Orphanet:3082)
Joubert syndrome with orofaciodigital defect (Orphanet:2754)
KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT (OMIM:118100)
KLIPPEL-FEIL SYNDROME 2, AUTOSOMAL RECESSIVE (OMIM:214300)
Kabuki syndrome (Orphanet:2322)
Kapur-Toriello syndrome (Orphanet:2328)
Kniest dysplasia (Orphanet:485)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
Langer-Giedion syndrome (Orphanet:502)
Larsen-like osseous dysplasia - short stature (Orphanet:2370)
Lateral meningocele syndrome (Orphanet:2789)
Lathosterolosis (Orphanet:46059)
Leigh syndrome (Orphanet:506)
MANDIBULOFACIAL DYSOSTOSIS WITH PTOSIS, AUTOSOMAL DOMINANT (OMIM:608257)
MICROTIA WITH MEATAL ATRESIA AND CONDUCTIVE DEAFNESS (OMIM:251800)
MURCS association (Orphanet:2578)
Malignant hyperthermia - arthrogryposis - torticollis (Orphanet:2215)
Mandibulofacial dysostosis-microcephaly syndrome (Orphanet:79113)
Marshall-Smith syndrome (Orphanet:561)
Metaphyseal dysostosis - intellectual deficit - conductive deafness (Orphanet:2502)
Monosomy 18q (Orphanet:1600)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 2, attenuated form (Orphanet:217093)
Multiple epiphyseal dysplasia, Beighton type (Orphanet:166011)
Multiple synostoses syndrome (Orphanet:3237)
Nager syndrome (Orphanet:245)
Nephrogenic diabetes insipidus - intracranial calcification (Orphanet:3145)
Nephrosis - deafness - urinary tract - digital malformations (Orphanet:2669)
Neuroectodermal syndrome, Johnson type (Orphanet:2316)
Non-rhizomelic chondrodysplasia punctata (Orphanet:176)
OCULODENTODIGITAL DYSPLASIA (OMIM:164200)
OROFACIODIGITAL SYNDROME VI (OMIM:277170)
OTOFACIOCERVICAL SYNDROME 1 (OMIM:166780)
OTOSCLEROSIS 1 (OMIM:166800)
Oculo-skeletal-renal syndrome (Orphanet:2716)
Oculoauriculovertebral spectrum with radial defects (Orphanet:2549)
Oculodentodigital dysplasia (Orphanet:2710)
Opitz G/BBB syndrome (Orphanet:2745)
Orofaciodigital syndrome type 2 (Orphanet:2751)
Orofaciodigital syndrome type 4 (Orphanet:2753)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Otofaciocervical syndrome (Orphanet:2792)
Otopalatodigital syndrome (Orphanet:669)
Otopalatodigital syndrome type 1 (Orphanet:90650)
Otopalatodigital syndrome type 2 (Orphanet:90652)
PARAGANGLIOMAS 1 (OMIM:168000)
PHAVER syndrome (Orphanet:2876)
PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES (OMIM:602249)
Patterson-Stevenson-Fontaine syndrome (Orphanet:2439)
Peters-plus syndrome (Orphanet:709)
Phocomelia - ectrodactyly - deafness - sinus arrhythmia (Orphanet:2878)
Postaxial acrofacial dysostosis (Orphanet:246)
Proximal symphalangism (Orphanet:3250)
RHYNS syndrome (Orphanet:140976)
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2 (OMIM:616331)
Ramon syndrome (Orphanet:3019)
Relapsing polychondritis (Orphanet:728)
Retinitis pigmentosa (Orphanet:791)
SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES (OMIM:602471)
SOTOS SYNDROME 1 (OMIM:117550)
SYMPHALANGISM, PROXIMAL, 1A (OMIM:185800)
Saethre-Chotzen syndrome (Orphanet:794)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Siegler-Brewer-Carey syndrome (Orphanet:3167)
Smith-Magenis syndrome (Orphanet:819)
Sotos syndrome (Orphanet:821)
Spondylocarpotarsal synostosis (Orphanet:3275)
Stapes ankylosis with broad thumbs and toes (Orphanet:140917)
Stickler syndrome (Orphanet:828)
TREACHER COLLINS SYNDROME 1 (OMIM:154500)
Thickened earlobes - conductive deafness (Orphanet:2405)
Thoracic dysplasia-hydrocephalus syndrome (Orphanet:1861)
Thrombocytopenia - Robin sequence (Orphanet:3323)
Treacher-Collins syndrome (Orphanet:861)
VAN MALDERGEM SYNDROME 1 (OMIM:601390)
VAN MALDERGEM SYNDROME 2 (OMIM:615546)
Waardenburg syndrome (Orphanet:3440)
Wolf-Hirschhorn syndrome (Orphanet:280)
X-linked mandibulofacial dysostosis (Orphanet:1131)
X-linked mixed deafness with perilymphatic gusher (Orphanet:383)
Zunich-Kaye syndrome (Orphanet:3474)