2026 ICD-10-CM Diagnosis Code I78.0Hereditary hemorrhagic telangiectasia
ICD-10-CM Codes›I00–I99›I70-I79›I78
- Billable — Valid for Submission
- Chronic Condition
I78.0 is a billable ICD-10-CM diagnosis code for hereditary hemorrhagic telangiectasia. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026) and groups to MS-DRG 299 through 301. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Other specified and unspecified circulatory disease.
Code Identity
Code Classification
Approximate SynonymsGuidance
Alternate terms and clinical phrases that map to this code.
- Abnormally short little finger
- Conjunctival telangiectasis
- Epilepsy telangiectasia syndrome
- Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome
- Hereditary benign telangiectasia
- Hereditary dysplasia of blood vessel
- Hereditary hemorrhagic telangiectasia of gingiva
- Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome
- Juvenile polyposis syndrome
- Juvenile polyposis syndrome with hereditary hemorrhagic telangiectasia
- Osler hemorrhagic telangiectasia syndrome
- Vascular abnormality of conjunctiva
Tabular List NotesGuidance
Coding notes and annotation back-references applicable to this code.
Inclusion Terms
- Rendu-Osler-Weber disease
These terms are the conditions for which that code is to be used. The terms may be synonyms of the code title, or, in the case of "other specified" codes, the terms are a list of the various conditions assigned to that code. The inclusion terms are not necessarily exhaustive. Additional terms found only in the Alphabetic Index may also be assigned to a code.
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
- Angioma - See Also: Hemangioma, by site;
- hemorrhagicum hereditaria - I78.0
- Angiomatosis - Q82.8
- hemorrhagic familial - I78.0
- hereditary familial - I78.0
- Disease, diseased - See Also: Syndrome;
- Epistaxis (multiple) - R04.0
- hereditary - I78.0
- Osler (-Weber)-Rendu disease - I78.0
- Rendu-Osler-Weber disease or syndrome - I78.0
- Syndrome - See Also: Disease;
- Osler-Weber-Rendu - I78.0
- Rendu-Osler-Weber - I78.0
- Telangiectasia, telangiectasis (verrucous) - I78.1
- familial - I78.0
- Weber-Osler syndrome - I78.0
External Cause of Injuries IndexGuidance
References for this code in the External Cause of Injuries Index.
- Angioma
- hemorrhagicum hereditaria
- Angiomatosis
- hemorrhagic familial
- Angiomatosis
- hereditary familial
- Babington's disease(familial hemorrhagic telangiectasia)
- Disease, diseased
- Babington's (familial hemorrhagic telangiectasia)
- Disease, diseased
- Goldstein's (familial hemorrhagic telangiectasia)
- Disease, diseased
- Osler-Rendu (familial hemorrhagic telangiectasia)
- Disease, diseased
- Rendu-Osler-Weber (familial hemorrhagic telangiectasia)
- Epistaxis(multiple)
- hereditary
- Goldstein's disease(familial hemorrhagic telangiectasia)
- Osler(-Weber)-Rendu disease
- Rendu-Osler-Weber disease or syndrome
- Syndrome
- Osler-Weber-Rendu
- Syndrome
- Rendu-Osler-Weber
- Telangiectasia, telangiectasis(verrucous)
- familial
- Telangiectasia, telangiectasis(verrucous)
- hemorrhagic, hereditary (congenital) (senile)
- Telangiectasia, telangiectasis(verrucous)
- hereditary, hemorrhagic (congenital) (senile)
- Weber-Osler syndrome
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Patient EducationClinical
Bleeding Disorders
Normally, if you get hurt, your body forms a blood clot to stop the bleeding. For blood to clot, your body needs cells called platelets and proteins known as clotting factors. If you have a bleeding disorder, you either do not have enough platelets or clotting factors or they don't work the way they should.
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
Convert I78.0 to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code HistoryHistory
Questions About I78.0Overview
Is I78.0 (Diseases of capillaries) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report hereditary hemorrhagic telangiectasia on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
What MS-DRG does I78.0 group to?
When hereditary hemorrhagic telangiectasia is the principal diagnosis on an inpatient stay, it groups to MS-DRG 299, 300, 301, with relative weights from 0.7197 to 1.6327 depending on complications. Higher weights mean higher Medicare reimbursement.
What is the ICD-9 equivalent of I78.0?
Under the General Equivalence Mappings, hereditary hemorrhagic telangiectasia converts to ICD-9-CM 448.0 (heredit hemorr telangiec). The mapping is a direct match.
Footnotes
[1] Chronic - a chronic condition code indicates a condition lasting 12 months or longer and its effect on the patient based on one or both of the following criteria:
- The condition results in the need for ongoing intervention with medical products,treatment, services, and special equipment
- The condition places limitations on self-care, independent living, and social interactions.
