ICD-10-CM Diagnosis Code I78.0
Effective Date: 10/01/2015 To 09/30/2025Hereditary hemorrhagic telangiectasia
| CMS-HCC-V24 | CMS-HCC-V28 | RxHCC | Age | Gender | Maternity | Acute or Chronic | MCC |
|---|---|---|---|---|---|---|---|
| 108 | -- | -- | -- | -- | -- | Acute | No |
Applicable To for I78.0:
Back-references to I78.0
Angioma see also Hemangioma, by site
Angiomatosis Q82.8
Babington's disease(familial hemorrhagic telangiectasia) I78.0
Disease, diseased see also Syndrome
Epistaxis(multiple) R04.0
Goldstein's disease(familial hemorrhagic telangiectasia) I78.0
Osler(-Weber)-Rendu disease I78.0
Rendu-Osler-Weber disease or syndrome I78.0
Syndrome see also Disease
Telangiectasia, telangiectasis(verrucous) I78.1
Weber-Osler syndrome I78.0
- hemorrhagicum hereditaria I78.0
- hemorrhagic familial I78.0
- hereditary familial I78.0
- Babington's(familial hemorrhagic telangiectasia) I78.0
- Goldstein's(familial hemorrhagic telangiectasia) I78.0
- Osler-Rendu(familial hemorrhagic telangiectasia) I78.0
- Rendu-Osler-Weber(familial hemorrhagic telangiectasia) I78.0
- hereditary I78.0
- Osler-Weber-Rendu I78.0
- Rendu-Osler-Weber I78.0
- familial I78.0
- hemorrhagic, hereditary(congenital) (senile) I78.0
- hereditary, hemorrhagic(congenital) (senile) I78.0
Chapter, Section and Diagnosis Prefix for
I78.0