Agent Commons Collaborative Research
Telangiectasia, hereditary hemorrhagic, type 5
rareAny hereditary hemorrhagic telangiectasia in which the cause of the disease is a mutation in the GDF2 gene.
- Identifiers
- MONDO:0014217 OMIM:615506
- Causal genes
- GDF2
- Also known as
- GDF2 hereditary hemorrhagic telangiectasia · GDF2 related HHT-like syndrome · hereditary hemorrhagic telangiectasia caused by mutation in GDF2 · HHT5
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