Edit ICD10 dx: Ear or hearing, congenital malformation

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{{ICD10 transition status | OldDxArticle = | CurrentStatus = reconciled | InitialEditorAssigned = not assigned }} == Additional Info == https://en.wikipedia.org/wiki/Congenital_hearing_loss '''Includes''' *Accessory auricle *Accessory tragus *Polyotia - auricular malformation (accessory ear) *Preauricular appendage *Supernumerary lobule or pinna *Macrotia/Microtia/Other misshapen ear (Pointed ear)/Misplaced ear(Low-set ears)/Prominent ear(Bat ear)/Congenital absence of lobe of ear *Combine with [[Chromosomal abnormality, NOS]] if appropriate '''TYPES of Hearing Malformation Include''' *Autosomal dominant hearing loss/Autosomal recessive hearing loss/X-linked hearing loss, combine with [[Hearing loss, any type]] *Combine with cause if known = Down syndrome (abnormality on a gene), Usher syndrome (autosomal recessive), Treacher Collins syndrome (autosomal dominant), Crouzon syndrome (autosomal dominant), and Alport syndrome (X-linked) *Other causes of congenital hearing loss that are not hereditary in nature include prenatal infections, illnesses, toxins consumed by the mother during pregnancy or other conditions occurring at the time of birth or shortly thereafter. These conditions typically cause sensorineural hearing loss ranging from mild to profound in degree. == Alternate ICD10s to consider coding instead or in addition == *[[Down syndrome (trisomy 21)]] *[[Malformation/disorder NOS, congenital]] *[[Chromosomal abnormality, NOS]] *[[Face and/or neck, congenital malformation]] *[[Eye, congenital malformation]] == Candidate [[Combined ICD10 codes]] == == Related CCI Codes == {{Data Integrity Check List}} == Related Articles == {{Related Articles}} {{ICD10 footer}} {{EndPlaceHolder}}

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