Abnormality of the auditory canal
Symptom Information:
Symptom ID: | HPO:0000372 | ||
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 outer ear(HPO:0000356) Abnormality of the auditory canal(HPO:0000372) MedDRA: |
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Database Frequency: | 49 / 7739 | ||
Resource: |
All diseases associated with this symptom:
14q22q23 microdeletion syndrome | (Orphanet:264200) |
16p13.11 microdeletion syndrome | (Orphanet:261236) |
Ablepharon macrostomia syndrome | (Orphanet:920) |
Acro-oto-ocular syndrome | (Orphanet:2980) |
BOR syndrome | (Orphanet:107) |
Barber-Say syndrome | (Orphanet:1231) |
Blepharophimosis-intellectual deficit syndrome, Ohdo type | (Orphanet:2728) |
Branchio-otic syndrome | (Orphanet:52429) |
Branchiogenic deafness syndrome | (Orphanet:50815) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cerebro-costo-mandibular syndrome | (Orphanet:1393) |
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) |
Coxoauricular syndrome | (Orphanet:1508) |
Craniodiaphyseal dysplasia | (Orphanet:1513) |
Craniofacial dyssynostosis | (Orphanet:1516) |
Crouzon disease | (Orphanet:207) |
Deafness - ear malformation - facial palsy | (Orphanet:3232) |
Ear-patella-short stature syndrome | (Orphanet:2554) |
Fine-Lubinsky syndrome | (Orphanet:1272) |
Fraser syndrome | (Orphanet:2052) |
Goldenhar syndrome | (Orphanet:374) |
Gonadal dysgenesis, XY type - associated anomalies | (Orphanet:1770) |
Holoprosencephaly - radial heart renal anomalies | (Orphanet:3186) |
Hypertelorism-microtia-facial clefting syndrome | (Orphanet:2213) |
Isotretinoin-like syndrome | (Orphanet:2306) |
Kapur-Toriello syndrome | (Orphanet:2328) |
Lambert syndrome | (Orphanet:1296) |
Lateral meningocele syndrome | (Orphanet:2789) |
Mandibulofacial dysostosis-microcephaly syndrome | (Orphanet:79113) |
Monosomy 9p | (Orphanet:261112) |
Mycophenolate mofetil embryopathy | (Orphanet:268249) |
Nager syndrome | (Orphanet:245) |
Neurofaciodigitorenal syndrome | (Orphanet:2673) |
Oculoauriculovertebral spectrum with radial defects | (Orphanet:2549) |
Otofaciocervical syndrome | (Orphanet:2792) |
Patterson-Stevenson-Fontaine syndrome | (Orphanet:2439) |
Pfeiffer syndrome type 2 | (Orphanet:93259) |
Pfeiffer syndrome type 3 | (Orphanet:93260) |
Phocomelia - ectrodactyly - deafness - sinus arrhythmia | (Orphanet:2878) |
Proteus syndrome | (Orphanet:744) |
Rasmussen-Johnsen-Thomsen syndrome | (Orphanet:3023) |
Recessive dystrophic epidermolysis bullosa inversa | (Orphanet:79409) |
Renal-genital-middle ear anomalies | (Orphanet:1092) |
Saethre-Chotzen syndrome | (Orphanet:794) |
Treacher-Collins syndrome | (Orphanet:861) |
Verloove Vanhorick-Brubakk syndrome | (Orphanet:3429) |