Cortexa research tool·genomics·mondo

Mondo Get Disease Phenotypes

Get HPO (Human Phenotype Ontology) phenotypes associated with a Mondo disease. Returns the phenotype IDs (HP:xxxxxxx), names, and the specific disease subtype contributing each phenotype. Data comes from OMIM, Orphanet, and clinical annotations. Use this to understand clinical presentations and symptoms of a disease. First find the Mondo ID using Mondo_search_disease, then query phenotypes here.

Livelast probed 2026-04-30 23:07Z· 112msCortexa

Status

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

Last probed: 1d ago
Last success: 1d ago
Last latency: 112ms

Schema

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

{
  "properties": {
    "disease_id": {
      "description": "Mondo disease identifier. Examples: 'MONDO:0004975' (Alzheimer disease, 95 phenotypes), 'MONDO:0005148' (type 2 diabetes, 50+ phenotypes), 'MONDO:0009061' (cystic fibrosis, 100+ phenotypes).",
      "type": "string"
    },
    "limit": {
      "description": "Maximum number of phenotypes to return (default: 20, max: 200).",
      "type": "integer"
    }
  },
  "required": [
    "disease_id"
  ],
  "type": "object"
}

Examples (1)

Default Mondo Get Disease Phenotypes call

public-safeinput

{
  "disease_id": "type 2 diabetes",
  "limit": 3
}

Expected response keys: success

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

Identifiers

Catalog ID: tu_Mondo_get_disease_phenotypes
Tool name: Mondo_get_disease_phenotypes
Added: 2026-04-30 22:47Z
Tags: tooluniverse

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