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OMIM (Online Mendelian Inheritance in Man) API Reference
OMIM (Online Mendelian Inheritance in Man) API Reference — reference document from Claude Code knowledge pack.
Claude Code Knowledge Pack7/10/2026
Overview
OMIM (Online Mendelian Inheritance in Man) API Reference
Base URL
https://api.omim.org/api
Authentication
API key REQUIRED. Request at https://omim.org/api (free for academic/non-commercial use).
- Pass as query parameter:
?apiKey=YOUR_API_KEY - All requests require the key; unauthenticated requests are rejected.
Rate Limits
Not publicly documented in detail. Reasonable usage expected per terms of service.
Response Format
JSON (with &format=json) or XML (default). Always append &format=json for JSON responses.
Key Endpoints
1. Entry Lookup (by MIM number)
GET https://api.omim.org/api/entry?mimNumber={mim_number}&apiKey={key}&format=json
Example:
GET https://api.omim.org/api/entry?mimNumber=141900&apiKey=YOUR_KEY&format=json
Returns entry with title, text, gene map, allelic variants, references.
2. Entry with Specific Includes
GET https://api.omim.org/api/entry?mimNumber=141900&include=text&include=allelicVariantList&include=geneMap&apiKey={key}&format=json
Include options: text, clinicalSynopsis, geneMap, allelicVariantList, referenceList, existFlags, externalLinks.
3. Search Entries
GET https://api.omim.org/api/entry/search?search={query}&apiKey={key}&format=json
Example — search for "Marfan syndrome":
GET https://api.omim.org/api/entry/search?search=marfan+syndrome&apiKey=YOUR_KEY&format=json&start=0&limit=10
4. Search with Filters
GET https://api.omim.org/api/entry/search?search={query}&filter=gene&apiKey={key}&format=json
Filter options: gene, phenotype, clinical_synopsis, etc.
5. Gene Map Lookup
GET https://api.omim.org/api/geneMap?chromosome={chrom}&apiKey={key}&format=json
Example:
GET https://api.omim.org/api/geneMap?chromosome=17&apiKey=YOUR_KEY&format=json&start=0&limit=10
6. Gene Map Search
GET https://api.omim.org/api/geneMap/search?search={query}&apiKey={key}&format=json
7. Clinical Synopsis Search
GET https://api.omim.org/api/clinicalSynopsis/search?search={query}&apiKey={key}&format=json
Response Structure
{
"omim": {
"version": "1.0",
"entryList": [
{
"entry": {
"mimNumber": 141900,
"status": "live",
"titles": {
"preferredTitle": "HEMOGLOBIN S; HBS",
"alternativeTitles": "SICKLE CELL ANEMIA"
},
"textSectionList": [...],
"geneMap": {
"chromosome": "11",
"cytoLocation": "11p15.4",
"geneSymbols": "HBB"
}
}
}
]
}
}
Pagination
Use start and limit query parameters:
&start=0&limit=20
MIM Number Types
- Asterisk (*): Gene
- Plus (+): Gene with known phenotype
- Number sign (#): Phenotype (molecular basis known)
- Percent (%): Phenotype (molecular basis unknown)
- Null: Other entry types
Notes
- OMIM data is copyrighted; API access is free for academic use but requires registration.
- The API does not support bulk downloads; use OMIM downloads page with separate agreement.
- Cross-reference MIM numbers with ClinVar, NCBI Gene, and HPO for integrated disease analysis.