Diagnosis Code

Q16.1 CONGENITAL ABSENCE, ATRESIA AND STRICTURE OF AUDITORY CANAL


Code Information

Diagnosis Code: Q16.1

Short Description: Congenital absence, atresia and stricture of auditory canal

Long Description: Congenital absence, atresia and stricture of auditory canal (external)

The code Q16.1 is VALID for claim submission

Code Classification:

  • Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
    • Congenital malformations of eye, ear, face and neck (Q10-Q18)
      • Congenital malform of ear causing impairment of hearing (Q16)
        • Q16.1 Congenital absence, atresia and stricture of auditory canal

Code Version: 2022 ICD-10-CM


Synonyms

  • Absence of ear canal
  • Bilateral congenital atresia of external ears
  • Bilateral congenital malformation of ears
  • Bilateral congenital malformation of ears
  • Bilateral congenital malformation of external ears
  • Bilateral congenital malformation of external ears
  • Bilateral congenital stenosis of external auditory canals
  • Congenital absence of auricle with atresia of auditory canal
  • Congenital absence of auricle with stenosis of auditory canal
  • Congenital absence of external auditory canal
  • Congenital anomaly of internal auditory canal
  • Congenital anomaly of internal auditory canal
  • Congenital anomaly of internal auditory canal
  • Congenital atresia of external auditory canal
  • Congenital atresia of external auditory canal
  • Congenital atresia of external auditory canal
  • Congenital atresia of external auditory canal
  • Congenital atresia of external auditory canal
  • Congenital atresia of left external ear
  • Congenital atresia of osseous meatus of middle ear
  • Congenital atresia of right external ear
  • Congenital stenosis of external auditory canal
  • Congenital stenosis of left external auditory canal
  • Congenital stenosis of right external auditory canal
  • Congenital stricture of external auditory canal
  • Congenital stricture of osseous meatus
  • Congenital stricture of osseous meatus of middle ear
  • Congenital vertical talus
  • Cooper Jabs syndrome
  • External auditory canal atresia, vertical talus, hypertelorism syndrome
  • Hypertelorism
  • Lesion of bilateral external ear canals
  • Persistent dislocation of joint
  • Rigid flat foot
  • Short stature, auditory canal atresia, mandibular hypoplasia, skeletal anomalies syndrome
  • X-linked external auditory canal atresia, dilated internal auditory canal, facial dysmorphism syndrome

Diagnostic Related Group(s)

The code Q16.1 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)
  • Other Ear, Nose, Mouth And Throat Diagnoses With Mcc (154)
  • Other Ear, Nose, Mouth And Throat Diagnoses With Cc (155)
  • Other Ear, Nose, Mouth And Throat Diagnoses Without Cc/mcc (156)

References to Index of Diseases and Injuries

The code Q16.1 has the following ICD-10-CM references to the Index of Diseases and Injuries
  • Inclusion Terms:
    • Congenital atresia or stricture of osseous meatus

Crosswalk Information

ICD-10 Code ICD-9 Code ICD-9 Description
Q16.1 Right Arrow 744.02 Ex ear anm NEC-impr hear

This ICD-10 to ICD-9 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-10 Code ICD-10 Description
Q16 Congenital malformations of ear causing impairment of hearing
Q16.0 Congenital absence of (ear) auricle
Q16.2 Absence of eustachian tube
Q16.3 Congenital malformation of ear ossicles
Q16.4 Other congenital malformations of middle ear
Q16.5 Congenital malformation of inner ear
Q16.9 Congenital malformation of ear causing impairment of hearing, unspecified


This page was last updated on: 10/1/2023