Ear or hearing, congenital malformation: Difference between revisions
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== Additional Info == | == 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]] == | == Candidate [[Combined ICD10 codes]] == | ||
== Related CCI Codes == | |||
{{Data Integrity Check List}} | |||
== Related Articles == | == Related Articles == | ||
{{Related Articles}} | {{Related Articles}} | ||
{{ICD10 footer}} | {{ICD10 footer}} | ||
{{EndPlaceHolder}} | {{EndPlaceHolder}} | ||
Latest revision as of 22:20, 21 January 2024
| 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.
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 Checks (automatic list)
none found
Related Articles
| Related articles: |
Show all ICD10 Subcategories