The Raras MCP server exposes a knowledge graph of rare diseases, enabling AI agents to query 10,468 diseases, HPO phenotypes, genes, SUS coverage, clinical trials, and scientific papers with traceable identifiers.
- Operator: Raras
- Endpoint: https://raras.org/api/mcp
- Transport: streamable-http
- Sign-in: No sign-in
- Category: AI and machine learning
- Use cases: Search rare diseases by name or symptoms; Check SUS medication coverage for specific conditions; Find active clinical trials in Brazil; Retrieve clinical details and phenotypes for a disease
- Tools: search_diseases, get_disease_detail, find_diseases_by_phenotypes, search_phenotypes, get_sus_coverage, find_reference_centers, find_active_trials, find_similar_diseases, find_phenotypically_similar, get_graph_stats, search_papers_semantic, find_papers_for_disease, analyze_clinical_case, get_schema, explain_relation, get_literature_relations, get_hypotheses, get_research_log, get_recent_updates, get_evidence
- Documentation: https://raras.org/mcp
- Directory listing: https://koskamo.com/explore/raras-mcp
- Also known as: Raras MCP MCP; raras-mcp