Cortexa research tool·clinical·omim

OMIM Search

Search OMIM database for Mendelian diseases and genes. OMIM is the authoritative source for human genetic disorders. Search by gene name, disease name, or phenotype keywords. Returns MIM numbers, titles, and entry types. Requires OMIM_API_KEY env var (register at omim.org/api).

Livelast probed 2026-04-30 23:07Z· 115msCortexa

Status

The most recent probe succeeded. Safe to call from the agent today.

Last probed: 1d ago
Last success: 1d ago
Last latency: 115ms

Schema

JSON Schema the agent (or your API call) must match.

{
  "properties": {
    "limit": {
      "default": 10,
      "description": "Maximum results (default: 10, max: 20)",
      "maximum": 20,
      "minimum": 1,
      "type": "integer"
    },
    "operation": {
      "const": "search",
      "description": "Operation type (fixed: search)",
      "type": "string"
    },
    "query": {
      "description": "Search query - gene name (BRCA1), disease (cystic fibrosis), or phenotype (intellectual disability)",
      "type": "string"
    },
    "start": {
      "default": 0,
      "description": "Offset for pagination (default: 0)",
      "type": "integer"
    }
  },
  "required": [
    "query"
  ],
  "type": "object"
}

Examples (1)

Default OMIM Search call

public-safeinput

{
  "limit": 3,
  "query": "BRCA1",
  "start": 1
}

Expected response keys: success

Anonymous-safe example. Rate-limited; no sign-in required.

Identifiers

Catalog ID: tu_OMIM_search
Tool name: OMIM_search
Added: 2026-04-30 22:47Z
Tags: tooluniverse

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