Also known as IgG4-related retroperitoneal fibrosis, IgG4-related disease, IgG4-related systemic disease, Ormond's disease, Sclerosing retroperitoneal granuloma, Albarran-Ormond syndrome, Ormond disease, Idiopathic retroperitoneal fibrosis
progressive condition characterized by deposition of fibrous tissue in the retroperitoneal space
via PubMed
Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).