Osler-Weber-Rondu syndrome (Hereditary Hemorrhagic Telangiectasia)
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.
Additional Info
This 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.[1][2]
Telangiectasia (small vascular malformations) may occur in the skin and mucosal linings of the nose and gastrointestinal tract.
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