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| References | OMIM | Gene | GeneReviews | HGMD | HGNC |
| GENATLAS PHENOTYPE |
| last update : 25-02-2009 |
| Symbol | ORW3 |
| Location | 5q31.3-q32 |
| Name | Rendu-Osler-Weber syndrome 3 |
| Other name(s) | hereditary hemorrhagic telangiectasia, type 3 |
| Other symbol(s) | HHT3 |
| Main clinical features | with pulmonary arteriovenous malformations |
| Genetic determination | autosomal dominant |
| Function/system disorder | hematology |
| cardiovascular | |
| Type | disease |
| Remark(s) |