monarch-database
Query the Monarch Initiative knowledge graph for disease-gene-phenotype associations across species.
Skill by lamm-mit
Install
Works with Claude Code, Claude apps, Codex, Cursor, Gemini CLI, GitHub Copilot, VS Code, OpenCode, Goose, Windsurf. Read the repository before you give any tool access to your data.
npx agentmarket install skill/lamm-mit-monarch-database
Asks which of your tools to add it to (Claude Code, Codex, Cursor, VS Code, Windsurf, Gemini CLI, Claude Desktop) and shows the change first. See https://agentmart.dev/cli.
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About
Use cases: backend
Reviews
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Permissions
What this skill can do and what it asks for, from its SKILL.md. Checked Oct 25, 2026.
- Tools
- No tools found
- Secrets
- None asked for
- Install scripts
- None found
Network hosts it talks to 1
codeload.github.com· found in install command
Files it touches
~/.claude/skills/monarch-database
What's inside
- Skill name
monarch-database- Description
- Query the Monarch Initiative knowledge graph for disease-gene-phenotype associations across species. Integrates OMIM, ORPHANET, HPO, ClinVar, and model organism databases. Use for rare disease gene discovery, phenotype-to-gene mapping, cross-species disease modeling, and HPO term lookup.
- License
- CC0-1.0
- Metadata
- skill-author: Kuan-lin Huang
- Instructions
- 29 lines in SKILL.md · view on GitHub
Files (1)
- SKILL.md
SKILL.md (first lines)
# Monarch Initiative Database ## Overview The Monarch Initiative (https://monarchinitiative.org/) is a multi-species integrated knowledgebase that links genes, diseases, and phenotypes across humans and model organisms. It integrates data from over 40 sources including OMIM, ORPHANET, HPO (Human Phenotype Ontology), ClinVar, MGI (Mouse Genome Informatics), ZFIN (Zebrafish), RGD (Rat), FlyBase, and WormBase. ## Core Capabilities The skill provides REST API v3 access for: 1. **Phenotype-to-gene mapping** - Find genes associated with human phenotype terms 2. **Disease-to-gene associations** - Discover disease-causing genes using MONDO disease identifiers 3. **Cross-species ortholog discovery** - Identify model organism orthologs for human genes 4. **HPO semantic similarity** - Compare phenotype profiles between individuals/organisms 5. **Automated disease diagnosis** - Build diagnostic algorithms from phenotype to gene lists ## Key Workflows - Rare disease gene discovery using patient phenotypes (HP terms) - Model organism selection for disease research - Phenotype-based patient stratification - Cross-species disease mechanism studies - Regulatory variant functional consequence prediction ## Best Practices Use standardized identifiers: MONDO for diseases, HP for phenotypes, HGNC for human genes. Leverage the integrated data from multiple curated sources for robust evidence accumulation.
From lamm-mit/scienceclaw, CC0-1.0.
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Signals
- Stars
- 250
- Forks
- 47
- Open issues
- 1
- Last commit (this folder)
- Mar 14, 2026 (7 months ago)
- Last release
- Jun 23, 2026 (4 months ago)
From GitHub (fetched Oct 24, 2026).
Details
- License
- CC0-1.0
- Repository
- github.com/lamm-mit/scienceclaw
- First seen
- Oct 24, 2026
- Last checked
- Oct 24, 2026
- Source
- GitHubgithub-graphql
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Cite this page
monarch-database skill. Agent Mart. https://agentmart.dev/skills/lamm-mit-monarch-database (last updated 2026-10-24)