MyDisease FAQs

Question 1

Which data sources does MyDisease integrate?

Accepted Answer

MyDisease aggregates data from key biomedical sources such as OMIM, Orphanet, DisGeNET, ClinVar, HPO, GWAS Catalog, CTD, KEGG, and UniProt, offering a rich, interconnected view of disease information.

Question 2

Can I use MyDisease for batch queries or data export?

Accepted Answer

Yes, MyDisease supports batch processing, allowing you to query up to 1000 diseases in a single request. You can also export your results in various formats including TSV, CSV, JSON, or Markdown.

Question 3

What is MyDisease and its primary function?

Accepted Answer

MyDisease is a Model Context Protocol (MCP) server that provides structured, programmatic access to the extensive MyDisease.info API. Its primary function is to offer a unified interface for comprehensive disease information.

Question 4

What types of disease information can I access through MyDisease?

Accepted Answer

You can access a wide range of information, including disease search by name, ID, symptom, gene associations, genetic variant analysis, phenotype mapping via HPO terms, clinical data (e.g., ClinVar), disease ontology, GWAS data, pathway analysis, drug information, and epidemiology.

Question 5

How do I get started with using the MyDisease MCP server?

Accepted Answer

To get started, first install Python 3.12+ along with 'uv' and 'mcpm' (MCP Manager). Then, use 'mcpm import' to add the MyDisease server to your preferred MCP client, such as Claude Desktop.

MyDisease

MyDisease

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