Q16.5: Congenital malformation of inner ear

You have a congenital malformation of the inner ear.

The ear is a sensory organ that is used to hear and to maintain one’s balance. There are 3 different areas in the ear: the outer ear, middle ear and inner ear.

The actual hearing organ, the cochlea, is in the inner ear. The cochlea consists of a channel of bone in a spiral, like a snail. Inside the cochlea are the sensory cells for hearing. The inner ear connects to the brain via the auditory nerve.

While developing in the womb, many different types of tissue develop in the body. The organs and body parts develop out of the various types of tissue. A child’s development in the womb being disrupted can cause malformations,

causing the inner ear to be missing or have an altered shape. Ear deformities can lead to poorer hearing with the affected ear or no hearing at all.

Additional indicator

On medical documents, the ICD code is often appended by letters that indicate the diagnostic certainty or the affected side of the body.

  • G: Confirmed diagnosis
  • V: Tentative diagnosis
  • Z: Condition after
  • A: Excluded diagnosis
  • L: Left
  • R: Right
  • B: Both sides

Further information

Note

This information is not intended for self-diagnosis and does not replace professional medical advice from a doctor. If you find an ICD code on a personal medical document, please also note the additional indicator used for diagnostic confidence.
Your doctor will assist you with any health-related questions and explain the ICD diagnosis code to you in a direct consultation if necessary.

Source

Provided by the non-profit organization “Was hab’ ich?” gemeinnützige GmbH on behalf of the Federal Ministry of Health (BMG).