Other congenital malformations of ear (Q17)

The ICD-10 code Q17 covers a range of specific congenital malformations of the ear, including abnormalities in ear shape, size, position, and structural formation present from birth. These codes help classify unique ear malformations for accurate medical documentation and billing.

The section includes detailed codes such as Q17.0 for accessory auricle, commonly known as preauricular appendage or accessory tragus; Q17.1 for macrotia, which refers to abnormally large ears; and Q17.2 for microtia, describing underdeveloped or unusually small ears often associated with hearing loss. Other codes include Q17.3 for various misshapen ear forms like lop ear or Vulcan ear, Q17.4 for misplaced or low-set ears, and Q17.5 for prominent ears, which are ears that stick out more than usual. The code Q17.8 covers other specified congenital ear malformations such as split ear lobes or congenital absence of the external auditory canal, and Q17.9 denotes unspecified congenital ear malformations. Understanding these codes ensures precise recording of conditions like accessory auricle or microtia, which are frequent entries when searching for the ICD-10 code for congenital ear anomalies.

Instructional Notations

Type 1 Excludes

A type 1 excludes note is a pure excludes note. It means "NOT CODED HERE!" An Excludes1 note indicates that the code excluded should never be used at the same time as the code above the Excludes1 note. An Excludes1 is used when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.

  • congenital malformations of ear with impairment of hearing Q16.0 Q16.9
  • preauricular sinus Q18.1

Clinical Terms

The following clinical terms provide additional context, helping users better understand the clinical background and common associations for each diagnosis listed in this section. Including related terms alongside ICD-10-CM codes supports coders, billers, and healthcare professionals in improving accuracy, enhancing documentation, and facilitating research or patient education.

Hypertelorism

Abnormal increase in the interorbital distance due to overdevelopment of the lesser wings of the sphenoid.

Microstomia

A congenital defect in which the mouth is unusually small. (Dorland, 27th ed)