hereditary hemorrhagic telangiectasia
MeSH: D013683ORPHA: 774
Overview
genetic disorder involving capillaries
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with hereditary hemorrhagic telangiectasia, sourced from HPO and Orphanet clinical annotations.
Lip telangiectasiaTongue telangiectasiaEpistaxisNasal mucosa telangiectasiaTelangiectasiaSpontaneous, recurrent epistaxisMucosal telangiectasiaeTelangiectasia of the skinPortal hypertensionAnemiaMigrainePulmonary arteriovenous malformationHepatic arteriovenous malformationAbnormal cardiovascular system physiologyArteriovenous malformationVisceral angiomatosisConjunctival telangiectasiaSeizureCerebral hemorrhageCirrhosisHepatic failureCongestive heart failureEsophageal varixPulmonary arterial hypertensionHemoptysisSubarachnoid hemorrhagePulmonary embolismGastrointestinal hemorrhageTransient ischemic attackCerebral arteriovenous malformationGastrointestinal arteriovenous malformationVenous thrombosisRetinal telangiectasiaAbnormal cerebral vascular morphologyPeripheral arteriovenous fistulaIntestinal polyposis
Classification & Codes
MeSH Code
D013683Orphanet Code
ORPHA:774hereditary hemorrhagic telangiectasia
| MeSH | D013683 |
| Orphanet | ORPHA:774 |
| Treatments | 0 drug(s) |
| Symptoms on record | 36 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO