Osler-Weber-Rondu syndrome (Hereditary Hemorrhagic Telangiectasia)

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ICD10 Diagnosis
Dx: Osler-Weber-Rondu syndrome (Hereditary Hemorrhagic Telangiectasia)
ICD10 code: I78.0
Pre-ICD10 counterpart: none assigned
Charlson/ALERT Scale: none
APACHE Como Component: none
APACHE Acute Component: none
Start Date:
Stop Date:
External ICD10 Documentation

This diagnosis is a part of ICD10 collection.

  • SMW
    • 2019-01-01
    • 2999-12-31
    • I78.0
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Additional Info

Osler-Weber-Rondu syndrome (Hereditary Hemorrhagic Telangiectasia / HHT) is a rare autosomal dominant genetic disorder that leads to abnormal blood vessel formation in the skin, mucous membranes, and often in organs such as the lungs, liver, and brain. Telangiectasia (small vascular malformations) may occur in the skin and mucosal linings of the nose and gastrointestinal tract. Arteriovenous malformation (AVM) is an abnormal connection between arteries and veins, bypassing the capillary system. This vascular anomaly is widely known because of its occurrence in the central nervous system (usually Arteriovenous malformation (AVM)), but can appear in any location. Although many AVMs are asymptomatic, they can cause intense pain or bleeding or lead to other serious medical problems.

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