I78.0
BillableHereditary hemorrhagic telangiectasia
Hereditary hemorrhagic telangiectasia
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Rendu-Osler-Weber disease
Excludes 2
Conditions not included here, but the patient may have both
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
- systemic connective tissue disorders (M30-M36)
- transient cerebral ischemic attacks and related syndromes (G45.-)
Also Known As / Clinical Terms
SNOMED CT
- Juvenile polyposis of intestine9273005
- Juvenile polyposis syndrome9273005
- Juvenile polyps of large bowel9273005
- Retention polyps of large bowel9273005
- HHT - Hereditary haemorrhagic telangiectasia21877004
- HHT - Hereditary hemorrhagic telangiectasia21877004
- Hereditary haemorrhagic telangiectasia21877004
- Hereditary hemorrhagic telangiectasia21877004
- Osler haemorrhagic telangiectasia syndrome21877004
- Osler hemorrhagic telangiectasia syndrome21877004
- Osler-Rendu-Weber disease21877004
- Osler-Rendu-Weber syndrome21877004
- Osler-Weber-Rendu disease21877004
- Conjunctival vascular abnormality74100001
- Vascular abnormality of conjunctiva74100001
- Conjunctival telangiectasis231870008
- Hereditary benign telangiectasia238764001
- Hereditary dysplasia of blood vessel461415008
- HLTRS (hypotrichosis, lymphedema, telangiectasia, renal defect) syndrome723363009
- HLTRS (hypotrichosis, lymphoedema, telangiectasia, renal defect) syndrome723363009
- Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome723363009
- Hypotrichosis, lymphoedema, telangiectasia, renal defect syndrome723363009
- Epilepsy telangiectasia syndrome733032006
- Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome782823001
- Abnormally short little finger897328006
- Shortened little finger897328006
- JP-HHT (juvenile polyposis with hereditary haemorrhagic telangiectasia) syndrome1149069001
- JP-HHT (juvenile polyposis with hereditary hemorrhagic telangiectasia) syndrome1149069001
- Juvenile polyposis syndrome with hereditary haemorrhagic telangiectasia1149069001
- Juvenile polyposis syndrome with hereditary hemorrhagic telangiectasia1149069001
- Hereditary haemorrhagic telangiectasia of gingiva1197033002
- Hereditary hemorrhagic telangiectasia of gingiva1197033002
UMLS
- HHTC0039445
- HHT - Hereditary haemorrhagic telangiectasiaC0039445
- HHT - Hereditary hemorrhagic telangiectasiaC0039445
- Hemorrhagic Telangiectasia, HereditaryC0039445
- Hereditary Hemorrhagic TelangiectasiaC0039445
- Hereditary haemorrhagic telangiectasiaC0039445
- Hereditary hemorrhagic telangiectasiaC0039445
- ORW DISEASEC0039445
- OSLER RENDU DISC0039445
- OSLER RENDU WEBER DISC0039445
- OSLER-RENDU-WEBER DISEASEC0039445
- Osler DiseaseC0039445
- Osler Rendu DiseaseC0039445
- Osler Rendu Weber DiseaseC0039445
- Osler Weber Rendu SyndromeC0039445
- Osler haemorrhagic telangiectasia syndromeC0039445
- Osler hemorrhagic telangiectasia syndromeC0039445
- Osler hemorrhagic telangiectasia syndrome (disorder)C0039445
- Osler's DiseaseC0039445
- Osler-Rendu DiseaseC0039445
- Osler-Rendu-Weber DiseaseC0039445
- Osler-Rendu-Weber diseaseC0039445
- Osler-Rendu-Weber syndromeC0039445
- Osler-Weber-Rendu DiseaseC0039445
- Osler-Weber-Rendu SyndromeC0039445
- Osler-Weber-Rendu diseaseC0039445
- Osler-Weber-Rendu syndromeC0039445
- Rendu Osler Weber DiseaseC0039445
- Rendu-Osler-Weber DiseaseC0039445
- Rendu-Osler-Weber diseaseC0039445
- Rendu-Osler-Weber syndromeC0039445
- TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBERC0039445
- Telangiectasia, Hereditary Hemorrahagic, of Rendu, OslerC0039445
- Telangiectasia, Hereditary HemorrhagicC0039445
- Telangiectasia, Hereditary Hemorrhagic, of Rendu, Osler, and WeberC0039445
- Weber Osler DiseaseC0039445
- Weber Osler SyndromeC0039445
- Weber-Osler DiseaseC0039445
- Weber-Osler SyndromeC0039445
- disease osler weber renduC0039445
- disease rendu-osler-weberC0039445
- hhtC0039445
- osler rendu syndrome weberC0039445
- osler rendu weberC0039445
- osler rendus syndrome weberC0039445
- osler weber renduC0039445
- osler weber rendu diseaseC0039445
- osler weber rendu syndromeC0039445
- osler's diseaseC0039445
- osler-rendu-weber syndromeC0039445
- osler-weber-rendu diseaseC0039445
- osler-weber-rendu syndromeC0039445
- rendu osler diseaseC0039445
- rendu osler weberC0039445
- rendu osler weber diseaseC0039445
- rendu osler weber syndromeC0039445
- rendu weber oslerC0039445
- rendu weber osler diseaseC0039445
- rendu-osler-weber diseaseC0039445
- rendu-osler-weber syndromeC0039445
Frequently Asked Questions
What is ICD-10 code I78.0?
ICD-10-CM code I78.0 represents "Hereditary hemorrhagic telangiectasia". It is a billable/specific code that can be used on a claim.
Is I78.0 a billable code?
Yes, I78.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is I78.0 in?
I78.0 is in Chapter 9: Diseases of the Circulatory System (codes I00-I99).
What SNOMED CT codes does I78.0 map to?
I78.0 maps to 12 SNOMED CT concepts: 897328006, 231870008, 74100001, 733032006, 782823001, and 7 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for I78.0?
I78.0 is linked to 1 UMLS Concept Unique Identifier: C0039445. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.