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).


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.
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.
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== Alternate ICD10s to consider coding instead or in addition ==
== Alternate ICD10s to consider coding instead or in addition ==
*[[Down syndrome (trisomy 21)]]
*[[Down syndrome (trisomy 21)]]
*[[Malformation/disorder NOS, congenital]]
*[[Chromosomal abnormality, NOS]]
== Candidate [[Combined ICD10 codes]] ==
== Candidate [[Combined ICD10 codes]] ==



Revision as of 12:44, 2018 June 29

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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Additional Info

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).


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

Candidate Combined ICD10 codes

Related CCI Codes

Related Articles

Related articles:


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