disease_phenotypes

Active

declared in 0.1.0

"What symptoms / clinical features does [disease] cause" / "HPO phenotypes for [OMIM N]" / "clinical signs of [rare disease]" — list HPO phenotype terms for a disease ID (OMIM:N, ORPHA:N, or MONDO:N format). Use to enumerate clinical features of rare diseases. Example ID: OMIM:154700 (Marfan syndrome).

Parameters schema

{
  "type": "object",
  "examples": [
    {
      "id": "OMIM:249000"
    },
    {
      "id": "ORPHA:558"
    }
  ],
  "required": [
    "id"
  ],
  "properties": {
    "id": {
      "type": "string"
    }
  }
}

What this tool wraps· 0 endpoints

min confidence0.70 0.50

No endpoints wrapped at confidence ≥ 0.50.

Parent server

Hpo Api

https://github.com/pipeworx-io/mcp-hpo-api

1/7 registries

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