Ear or hearing, congenital malformation: Difference between revisions

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== Related CCI Codes ==
== Related CCI Codes ==
{{Data Integrity Check List}}


== Related Articles ==
== Related Articles ==
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{{Related Articles}}


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Revision as of 23:48, 2018 November 17

ICD10 Diagnosis
Dx: Ear or hearing, congenital malformation
ICD10 code: Q17
Pre-ICD10 counterpart: none assigned
Charlson/ALERT Scale: none
APACHE Como Component: none
APACHE Acute Component: none
Start Date:
Stop Date:
External ICD10 Documentation

This diagnosis is a part of ICD10 collection.

  • SMW
    • 2019-01-01
    • 2999-12-31
    • Q17
  • Cargo


  • Categories
  • SMW
  • Cargo


  • Categories
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  • Categories

Additional Info

https://en.wikipedia.org/wiki/Congenital_hearing_loss

CAUSES of Ear/Hearing Congenital Malformation= Down syndrome (abnormality on a gene), Usher syndrome (autosomal recessive), Treacher Collins syndrome (autosomal dominant), Crouzon syndrome (autosomal dominant), and Alport syndrome (X-linked).

TYPES of Hearing Malformation are /Autosomal dominant hearing loss/Autosomal recessive hearing loss/X-linked hearing loss/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.

Other congenital malformations of ear =Accessory auricle/Accessory tragus/Polyotia/Preauricular appendage or tag/Supernumerary:ear/lobule/ Macrotia/Microtia/Other misshapen ear (Pointed ear)/Misplaced ear(Low-set ears)/Prominent ear(Bat ear)/Congenital absence of lobe of ear


Alternate ICD10s to consider coding instead or in addition

Candidate Combined ICD10 codes

Related CCI Codes

Data Integrity Checks (automatic list)

none found

Related Articles

Related articles:


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