Abnormality of the auditory canal

Symptom Information:

Symptom ID: HPO:0000372
Auditory canal abnormality [HPO:0000372]
Cross references:
Is a (Direct Parents):
HPO         Abnormality of the outer ear
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the ear(HPO:0000598)
          Abnormality of the outer ear(HPO:0000356)
             Abnormality of the auditory canal(HPO:0000372)
Database Frequency: 49 / 7739

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)