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The Human Phenotype Ontology in 2017., , , , , , , , , and 49 other author(s). Nucleic Acids Research, 45 (Database-Issue): D865-D876 (2017)Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources., , , , , , , , , and 59 other author(s). Nucleic Acids Research, 47 (Database-Issue): D1018-D1027 (2019)OntoOrpha: An Ontology to Support Edition and Audit of Knowledge of Rare Diseases in ORPHANET., , , , , , , and . ICBO, volume 833 of CEUR Workshop Proceedings, CEUR-WS.org, (2011)CEMARA: a Web Dynamic Application Within a N-tier Architecture for Rare Diseases., , , , , , , , , and 6 other author(s). MIE, volume 136 of Studies in Health Technology and Informatics, page 51-56. IOS Press, (2008)Mapping Orphanet Terminology to UMLS., , , and . AIME, volume 6747 of Lecture Notes in Computer Science, page 194-203. Springer, (2011)