Cortexa research tool·genomics·mondo

Mondo Get Disease

Get detailed information about a disease from the Mondo Disease Ontology by its MONDO ID. Returns the disease name, description, synonyms, cross-references (OMIM, Orphanet, DOID, MeSH, ICD-10, NCIT, UMLS, SNOMED-CT), hierarchy (parent diseases), subtypes count, causal genes, inheritance pattern, and association counts (phenotypes, correlated genes, etc.). Essential for understanding disease classification and finding equivalent IDs across ontologies.

Livelast probed 2026-04-30 23:07Z· 90msCortexa

Status

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

Last probed: 1d ago
Last success: 1d ago
Last latency: 90ms

Schema

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

{
  "properties": {
    "disease_id": {
      "description": "Mondo disease identifier. Examples: 'MONDO:0004975' (Alzheimer disease), 'MONDO:0005148' (type 2 diabetes mellitus), 'MONDO:0007254' (breast cancer), 'MONDO:0018076' (Huntington disease), 'MONDO:0009061' (cystic fibrosis).",
      "type": "string"
    }
  },
  "required": [
    "disease_id"
  ],
  "type": "object"
}

Examples (1)

Default Mondo Get Disease call

public-safeinput

{
  "disease_id": "type 2 diabetes"
}

Expected response keys: success

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

Identifiers

Catalog ID: tu_Mondo_get_disease
Tool name: Mondo_get_disease
Added: 2026-04-30 22:47Z
Tags: tooluniverse

Back to catalog