Conductive hearing impairment
Symptom Information:
Symptom ID: | HPO:0000405 | ||||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | |||||||||||||||||||||||||||||||||
Cross references: |
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Is a (Direct Parents): | |||||||||||||||||||||||||||||||||
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) |
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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) |