"Projects and Programs Written in Rust" matching MCP servers:

MyChart MCP Server

An MCP server that grounds protein research in the UniProt SPARQL endpoint, providing tools for querying proteins, sequences, variants, diseases, and more via intent-named tools and raw SPARQL.

Grounds gene-nomenclature work in the HUGO Gene Nomenclature Committee (HGNC) dataset, enabling resolution of gene symbols and IDs to canonical HGNC identifiers, plus cross-references and batch operations.

Renders interactive 2D molecular structure diagrams from SMILES notation and computes molecular properties like molecular weight, LogP, and TPSA, directly in the chat.

Search 200M+ patents and scientific literature in natural language using PatSnap's global R&D intelligence database.

Enables AI assistants to answer healthcare REIT portfolio questions with deterministic, provable answers grounded in Omega Healthcare 10-K filings and CMS nursing home data, including status, caveats, and provenance.

A Claude Code extension that embeds a senior athenahealth integration engineer in your development workflow, proactively catching data loss bugs and guiding safe DataView queries and API integrations.

A Model Context Protocol (MCP) server for searching the National Provider Identifier (NPI) registry. This server provides tools to search and retrieve information about healthcare providers and organizations in the United States.

Enables AI assistants to upload clinical documents and medical device images for health data extraction, normalization, and retrieval of structured coded results in formats such as JSON, FHIR, HL7, CSV, and Parquet.

Enables searching and retrieving molecular hydrogen medical literature from H2 Papers database, with per-paper safety notes always included in results.

A Claude-compatible MCP server that exposes health-domain tools over 100% synthetic data, built with security and compliance in mind.

Exposes four CMS public datasets as callable tools in Claude conversations, enabling natural-language real-world evidence analytics without SQL expertise.

Provides access to the Human Phenotype Ontology (HPO) API with tools for searching, browsing hierarchy, and analyzing phenotypic terms used in genetic research.

Enables healthcare AI interactions via MCP protocol with built-in EU AI Act compliance. Provides quick installation, well-documented API, and enterprise support.

MCP server and CLI for detecting, redacting, and auditing PHI in medical text before it reaches AI agents.

MCP server and CLI for detecting, redacting, and auditing PHI in medical text before it is sent to AI agents, with tools for scan, redact, audit, and validate operations.

A fastmcp-based tool for writing prompts against data in the NMDC database.

Provides read/write access to any FHIR-compliant healthcare API with built-in validation, supporting resource management, search operations, and granular permissions through natural language.

Provides seamless access to the Protein Data Bank in Europe (PDBe) API and search capabilities, enabling AI clients to query protein structures, perform advanced searches, and retrieve structural biology data.

Enables AI-powered genomic variant analysis including variant impact prediction, regulatory element discovery, and batch variant scoring. Currently operates in mock mode as a proof-of-concept awaiting the public release of Google DeepMind's AlphaGenome API.