Q80.8: Other congenital ichthyosis
You have a congenital skin disorder where the skin cells do not keratinize properly.
The top of layer of skin is made up of skin cells that are keratinized. These skin cells are initially in one of the lower skin layers. When the skin cells migrate upwards toward the skin’s surface, they keratinize, forming a solid layer.
The genetic information in your cells has changed. This disrupts the keratinization of your skin.
Your skin may form scales, blisters or hard patches, for example. It is also possible for the skin to be very red or for it to become inflamed more easily than usual. You can also have various other symptoms.
This disease can be hereditary. Other family members may also be affected.
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).