"Exploration of the term '.core' and its references" matching MCP servers:

Enables LLM-based agents to interact with FHIR healthcare data through natural language prompts, providing full CRUD operations on FHIR resources, document processing, and semantic search capabilities.

Enables AI agents to resolve and cross-reference biological entities such as genes, proteins, and aliases across authoritative databases like HGNC, NCBI Entrez, and UniProt, with confidence scores and source citations.

Resolves free-text condition and disease strings — trial-registry condition fields, drug-label indications, hand-typed wording — onto the Mondo Disease Ontology, returning the best term id and label along with a trustworthy match-quality label (exact label/synonym, broader, narrower, fuzzy, or no-match) plus cross-ontology xrefs. Optionally expands a resolved term to all of its descendant ids for building subtype-inclusive registry filters.

Provides secure access to VA's VistA electronic health record system, enabling AI applications to retrieve and summarize patient medical records for clinical staff.

Explains why two scientific papers disagree. A contradiction explorer for bench scientists that compares two studies' designs and grounds every claim in a verbatim quote from the source text.

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.

Enables semantic retrieval and assembly of ICD-10-CM value sets from natural language descriptions for clinical cohort definitions.

Connects Claude to the U.S. National Library of Medicine MeSH APIs to search and retrieve medical authority data, descriptors, and qualifiers. It enables library and metadata staff to perform subject analysis and confirm terminology within an AI-assisted cataloging workflow.

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.

An MCP server implementing the ROBINS-I V2 framework for risk-of-bias assessment in non-randomized studies, with deterministic algorithms and full provenance. It enables users to parse study documents, specify target trial results, answer signalling questions with evidence-bound quotes, and compute or override domain judgements.

Enables querying and monitoring Brazilian Federal Council of Medicine resolutions on AI, telemedicine, and electronic medical records, with a local searchable copy and official document links.

MyChart MCP Server

MCP server that reads glucose data from a FreeStyle sensor via the LibreLinkUp API, providing current glucose and history with explicit coverage and gaps.

Enables natural language querying of brain volumes (NIfTI) with a fixed set of tools, returning visualizations and reproducible nilearn code.

Privacy layer for healthcare AI agents. Pseudonymises patient identifiers (NHS numbers, names, dates of birth, addresses; UK and US) into labelled tokens locally before text reaches an agent, then restores the originals afterwards, keeping the token map out of agent context.

Enables automated assessment of research manuscripts against the TARGET reporting guideline for target trial emulation, providing item-by-item scoring with evidence and provenance.

MCP server for automated ICD-10 medical coding. Code clinical text to ICD-10-CM diagnoses, search 74,000+ codes, and de-identify PHI via the AutoICD API.

MCP server for the Swiss Federal Office of Public Health Infectious Disease Dashboard, providing access to epidemiological surveillance data for 51 pathogens across Switzerland, including influenza, COVID-19, measles, and wastewater surveillance.

Local MCP server to access your personal health data from E-Nabız (Turkish Ministry of Health) via an LLM. Read-only, secure, and respects privacy.

Enables coding agents to interact with the Reactome pathway database, including search, lookup, hierarchy traversal, SBML/SBGN export, and gene-set enrichment analysis.