Hereditary hemorrhagic telangiectasia
Billable / specific
I78.0 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.
Inclusion terms
Applicable to
- Rendu-Osler-Weber disease
Excludes2
Not included here — may be reported together when both conditions exist.
- certain conditions originating in the perinatal period (P04-P96) (from I78)
- certain infectious and parasitic diseases (A00-B99) (from I78)
- complications of pregnancy, childbirth and the puerperium (O00-O9A) (from I78)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99) (from I78)
- endocrine, nutritional and metabolic diseases (E00-E88) (from I78)
- injury, poisoning and certain other consequences of external causes (S00-T88) (from I78)
- neoplasms (C00-D49) (from I78)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94) (from I78)
- systemic connective tissue disorders (M30-M36) (from I78)
- transient cerebral ischemic attacks and related syndromes (G45.-) (from I78)
Also known as
- Rendu-Osler-Weber disease
- Angioma, hemorrhagicum hereditaria
- Angiomatosis, hemorrhagic familial
- Angiomatosis, hereditary familial
- Babington's disease
- Disease, diseased, Babington's
- Disease, diseased, Goldstein's
- Disease, diseased, Osler-Rendu
- Disease, diseased, Rendu-Osler-Weber
- Epistaxis, hereditary
- Goldstein's disease
- Osler-Rendu disease
- Rendu-Osler-Weber disease or syndrome
- Syndrome, Osler-Weber-Rendu
- Syndrome, Rendu-Osler-Weber
- Telangiectasia, telangiectasis, familial
Parent code
- I78Diseases of capillariesHeader