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:
Data Dependencies(Reports/Indicators/Data Elements):	No results
External ICD10 Documentation	ICD-10 CM Wikipedia ICD-10 Wikipedia WHO ICD10 documentation ICD10data.com

This diagnosis is a part of ICD10 collection.

Additional Info

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.

Skin	Trauma	Renal/urinary	Infectious disease
ENT	Testing	Cardiovascular	Hereditary/congenital
Eye	Mechanism	Neoplastic	Heme/immunology
Misc	Reproductive	Gastrointestinal	Musculoskeletal/soft tissue
Psych	Respiratory	Poisoning
Neuro	Symptom/Sign	Endocrine disorder