Retrieve drug-gene interactions and pharmacogenomics data from PharmGKB by querying genes, drugs, or variants.
MIT
261,453 tools. Last updated 2026-07-05 12:39
"Research on Patient-Disease-Gene-Drug Relationships and Pharmacogenomics Using Digital Imaging Data" matching MCP tools:
- Run a comprehensive genomic report covering pharmacogenomics, disease risk for 19 conditions, and 30+ genetic traits with evidence, odds ratios, and citations.MIT
- Generate a complete genomic intelligence report combining medication pharmacogenomics, disease risk assessment, and trait analysis for personalized health insights.MIT
- Search FDA adverse event reports by drug name. Filter by reaction to retrieve seriousness, demographics, and drug information.MIT
- Retrieve comprehensive biomedical data for articles, clinical trials, genes, drugs, diseases, and variants using unique identifiers. Standardized format supports detailed research and analysis across domains.MIT
- Retrieve all recorded patient allergies to identify substances to avoid and enable safe drug interaction checks.MIT
Matching MCP Servers
- AlicenseAqualityBmaintenanceEnables searching and retrieving Korean disease information and statistics from the Health Insurance Review and Assessment Service (HIRA) using Claude.Last updated5MIT
- Alicense-qualityBmaintenanceMade-to-order data for AI agents via x402 micropayments on Base. Describe a need in plain language, get a custom quote, pay per call. No signup, no API keys. HTTP + MCP transports. 5 tools.Last updatedMIT
Matching MCP Connectors
Disease MCP — wraps disease.sh API (COVID-19 statistics, no auth required)
1k patient MCP server
- Execute pre-built queries on Alliance of Genome Resources data to retrieve gene orthologs, GO terms, disease associations, and other genomic information using parameterized templates.MIT
- Retrieve a structured dossier of a UniProt entry for drug-discovery workflows, summarizing identity, function, structure, drug targets, disease associations, and variants to guide further analysis.Apache 2.0
- Search PubMed for peer-reviewed biomedical literature on research papers, drug mechanisms, and clinical studies. Returns up to 10 results per query.MIT
- Retrieve detailed gene annotations, including names, summaries, aliases, types, and database links from MyGene.info. Use for accurate, real-time gene information on symbols or IDs like TP53 or BRAF.MIT
- Retrieve comprehensive disease details, including definitions, synonyms, ontology mappings, and associated phenotypes, directly from MyDisease.info via BioMCP. Ideal for precise biomedical research.MIT
- Search FDA Adverse Event Reporting System (FAERS) to identify drug side effects, serious reactions, and safety signals across patient populations. Use to gather insights from voluntary reports on adverse drug events.MIT
- Search FDA drug adverse event reports to identify side effects and patient reactions using openFDA data with quality scoring and audit verification.
- Look up clinical significance and pathogenicity of genetic variants. Find variants associated with diseases and research gene-disease associations.Apache 2.0
- Analyze gene lists to identify overrepresented biological processes using Gene Ontology enrichment, helping interpret gene expression data and uncover functional implications.MIT
- Search Swiss notifiable animal disease cases by canton and year to report on disease occurrence since 1991.MIT
- Retrieve a complete pharmacogenomics panel across 34 CPIC pharmacogenes. Derives star alleles from genotypes at key variant positions, providing a comprehensive starting point for pharmacogenomic analysis.MIT
- Retrieve diseases associated with a gene by providing its HGNC symbol. Automatically queries DisGeNET or OpenTargets databases.MIT
- Check insurance eligibility for a Tebra patient by examining active policies and authorization history from on-file data.MIT
- Fetch a protein's UniProt entry by accession to obtain its function, gene, organism, disease associations, and cross-references.Apache 2.0