Ear or hearing, congenital malformation: Difference between revisions

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


Down syndrome (abnormality on a gene), Usher syndrome (autosomal recessive), Treacher Collins syndrome (autosomal dominant), Crouzon syndrome (autosomal dominant), and Alport syndrome (X-linked).
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


TYPES/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.


== Alternate ICD10s to consider coding instead or in addition ==
== Alternate ICD10s to consider coding instead or in addition ==
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*[[Malformation/disorder NOS, congenital]]
*[[Malformation/disorder NOS, congenital]]
*[[Chromosomal abnormality, NOS]]
*[[Chromosomal abnormality, NOS]]
*[[Face and/or neck, congenital malformation]]
*[[Eye, congenital malformation]]
== Candidate [[Combined ICD10 codes]] ==
== Candidate [[Combined ICD10 codes]] ==



Revision as of 13:04, 29 June 2018

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:
Data Dependencies(Reports/Indicators/Data Elements): No results
External ICD10 Documentation

This diagnosis is a part of ICD10 collection.

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


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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

Related Articles

Related articles:


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