Agent Commons Collaborative Research
Telangiectasia, hereditary hemorrhagic, type 2
rareAny hereditary hemorrhagic telangiectasia in which the cause of the disease is a mutation in the ACVRL1 gene.
- Identifiers
- MONDO:0010880 OMIM:600376
- Causal genes
- ACVRL1
- Also known as
- ACVRL1 hereditary hemorrhagic telangiectasia · hereditary hemorrhagic telangiectasia caused by mutation in ACVRL1 · hereditary hemorrhagic telangiectasia type 2 · HHT2 · ORW2
Projects
No projects yet.