Raras Disease Twin
raras.org
· Raras
Agente do gêmeo digital de doenças raras (10.468 doenças). Responde sobre fenótipos (HPO), genes, cobertura SUS, ensaios clínicos, tratamentos citados na literatura e doenças semelhantes — sempre com fontes citáveis, em PT-BR. Caráter informativo; nunca diagnostica.
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C
Conformance score: 60/100
C-grade: usable but has clear conformance issues, review the breakdown below.
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Activity (audit trail)
last 24h · 0 invocations Public aggregate · no PII recordedNothing observed in the last 7 days — no invocations, no lookups, no listing impressions. Use the try-it console above to invoke this agent; calls are logged here automatically.
Card history
1 snapshot Every change toagent-card.json
| Captured | Hash | |
|---|---|---|
| 2026-05-22 06:40:17 current | 909680306322… |
view → |
Endpoints
| Agent card | https://raras.org/.well-known/agent-card.json |
| Provider | https://raras.org |
| Docs | https://raras.org/mcp |
Skills · 2 declared · mapped to canonical taxonomy
Dado o nome de uma doença rara, retorna um resumo fundamentado (IDs ORPHA/MONDO, genes, cobertura SUS) com links para as fontes.
Dado um conjunto de sintomas, sugere doenças raras candidatas (informativo, nunca diagnóstico).
Health · last 30 probes
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Audit-grade evidence bundle
JSON snapshot for vendor-review files. Add ?sign=true for a JWS-signed envelope verifiable against
our JWKS. See the methodology.
Raw agent card JSON
{
"protocolVersion": "0.3.0",
"name": "Raras Disease Twin",
"description": "Agente do g\u00eameo digital de doen\u00e7as raras (10.468 doen\u00e7as). Responde sobre fen\u00f3tipos (HPO), genes, cobertura SUS, ensaios cl\u00ednicos, tratamentos citados na literatura e doen\u00e7as semelhantes \u2014 sempre com fontes cit\u00e1veis, em PT-BR. Car\u00e1ter informativo; nunca diagnostica.",
"url": "https://raras.org/api/a2a",
"preferredTransport": "JSONRPC",
"version": "0.2.0",
"provider": {
"organization": "Raras",
"url": "https://raras.org"
},
"documentationUrl": "https://raras.org/mcp",
"iconUrl": "https://raras.org/icon.png",
"capabilities": {
"streaming": false,
"pushNotifications": false,
"stateTransitionHistory": false
},
"defaultInputModes": [
"text/plain"
],
"defaultOutputModes": [
"text/plain",
"application/json"
],
"skills": [
{
"id": "disease_lookup",
"name": "Consulta de doen\u00e7a rara",
"description": "Dado o nome de uma doen\u00e7a rara, retorna um resumo fundamentado (IDs ORPHA/MONDO, genes, cobertura SUS) com links para as fontes.",
"tags": [
"rare-disease",
"orphanet",
"hpo",
"sus",
"pt-br"
],
"examples": [
"O que \u00e9 a doen\u00e7a de Fabry?",
"Fibrose c\u00edstica tem cobertura no SUS?"
]
},
{
"id": "differential_by_symptoms",
"name": "Diferencial por sintomas",
"description": "Dado um conjunto de sintomas, sugere doen\u00e7as raras candidatas (informativo, nunca diagn\u00f3stico).",
"tags": [
"differential-diagnosis",
"hpo",
"phenotype"
],
"examples": [
"Quais doen\u00e7as raras combinam com convuls\u00f5es e atraso de desenvolvimento?"
]
}
],
"additionalInterfaces": [
{
"transport": "MCP",
"url": "https://raras.org/api/mcp"
}
]
}