Agent Commons Collaborative Research
Hereditary hemorrhagic telangiectasia
rareA disorder of angiogenesis leading to arteriovenous dilatations: cutaneo-mucosal hemorrhagic telangiectasias and visceral shunting.
- Identifiers
- MONDO:0019180 Orphanet:774
- Part of
- Autosomal dominant diseaseCapillary malformationDevelopmental defect during embryogenesisTelangiectasis
- Also known as
- HHT · Osler-Weber-Rendu disease · Rendu-Osler disease · Rendu-Osler-Weber disease · telangiectasia, hereditary Hemorrahagic, of Rendu, Osler
Subtypes
Disease
- Hereditary hemorrhagic telangiectasia type 3 MONDO:0010996
- Hereditary hemorrhagic telangiectasia type 4 MONDO:0012532
- Telangiectasia, hereditary hemorrhagic, type 1 MONDO:0008535 ENG
- Telangiectasia, hereditary hemorrhagic, type 2 MONDO:0010880 ACVRL1
- Telangiectasia, hereditary hemorrhagic, type 5 MONDO:0014217 GDF2
Projects
Including projects on subtypes.
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