Ear or hearing, congenital malformation: Difference between revisions
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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.
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
- 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
Show all ICD10 Subcategories