Ear or hearing, congenital malformation

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	ICD-10 CM Wikipedia ICD-10 Wikipedia WHO ICD10 documentation ICD10data.com

This diagnosis is a part of ICD10 collection.

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

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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

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