medical-records

Manage medical and genomic records through a health-graph-mcp.

15|7|Updated Aug 6, 2025
One-click install
npx skills add https://github.com/hvkshetry/StewardOS --skill medical-records
Or copy as Structured Prompt for Agent
Please help me install this Agent Skill.
Skill: medical-records
Source: https://github.com/hvkshetry/StewardOS/tree/main/skills/personas/wellness-advisor/medical-records
Command: npx skills add https://github.com/hvkshetry/StewardOS --skill medical-records

SYSTEM DOCUMENTATION & REQUIREMENTS

💡 This Skill includes references (resource) components.

What problem does it solve?

This Skill streamlines the management of sensitive medical and genomic data, enabling efficient ingestion, querying, and analysis of health-related information.

Core Features & Use Cases

  • Data Ingestion: Handles various health artifacts including genome data, lab results, and coverage information.
  • PGx Analysis: Facilitates querying of pharmacogenomic profiles and evaluating coverage for medical procedures.
  • Document Linking: Connects disparate health documents and evidence for comprehensive record-keeping.

Quick Start

Use the medical-records skill to ingest genome raw data from the attached file 'genome_data.vcf'.

Frequently Asked Questions about medical-records

High-intent search queries and answers about installing and using this skill.

FAQPage Schema
How do I ingest and query FHIR medical records?

The Skill supports FHIR data ingestion to manage medical records, allowing you to ingest genome and lab artifacts, query pharmacogenomic profiles, and link health documents within a health-graph-mcp environment.

Can I analyze pharmacogenomic profiles from raw genome data?

Yes, you can analyze pharmacogenomic profiles by executing the PGx pipeline to ingest raw genome data, query specific variants, and evaluate coverage for medical procedures and devices.

How do I evaluate coverage for medical procedures and devices?

You evaluate coverage for procedures and devices by ingesting coverage artifacts into the health-graph-mcp, which then links the evidence to the relevant subject's medical and genomic records.

Does this tool support linking disparate health documents and evidence?

Yes, document linking connects disparate health documents and evidence, streamlining the management of sensitive medical data by enabling comprehensive record-keeping across genome and lab results.

What is required to start managing genomic records and lab results?

To start managing genomic records, you need to ingest raw genome data, such as from an attached VCF file, into the health-graph-mcp to enable variant querying and PGx pipeline execution.

Are there limitations when handling sensitive medical and genomic data?

The Skill streamlines managing sensitive medical and genomic data by ingesting artifacts and executing PGx pipelines, though users must ensure proper environment setup to handle FHIR data and coverage evaluations securely.