raras
Server Details
Disease Twin — Brazil's rare-disease knowledge graph (10,468) over MCP. Source-grounded, PT-BR.
- Status
- Healthy
- Last Tested
- Transport
- Streamable HTTP
- URL
- Repository
- rarasAI/raras
- GitHub Stars
- 0
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Tool Definition Quality
Score is being calculated. Check back soon.
Available Tools
21 toolsanalyze_clinical_caseAnalisar caso clínicoRead-onlyInspect
Caso clínico → doenças candidatas + literatura relevante em 1 chamada. Apenas informativo, nunca diagnóstico.
| Name | Required | Description | Default |
|---|---|---|---|
| papers_limit | No | ||
| diseases_limit | No | ||
| case_description | Yes |
explain_relationExplicar relação (MedGraphRAG, raciocínio multi-hop)Read-onlyInspect
Raciocínio fundamentado sobre o grafo: dada uma pergunta (ex.: "por que o gene X se associa à doença Y?", "como a droga Z se relaciona a esta doença?"), retorna caminhos de evidência multi-hop (doença↔gene↔via↔droga↔fenótipo) com proveniência citável. Se não houver caminho no grafo, recusa — nunca inventa.
| Name | Required | Description | Default |
|---|---|---|---|
| query | Yes | ||
| hpo_ids | No | ||
| max_hops | No |
Output Schema
| Name | Required | Description |
|---|---|---|
| paths | Yes | |
| query | Yes | |
| summary | Yes | |
| hasEvidence | Yes |
find_active_trialsEnsaios clínicos ativosInspect
Trials ativos com filtro Brazil.
| Name | Required | Description | Default |
|---|---|---|---|
| limit | No | ||
| orphaCode | Yes | ||
| in_brazil_only | No |
find_communitiesComunidades de pacientesInspect
Comunidades FEBRARARAS por doença.
| Name | Required | Description | Default |
|---|---|---|---|
| limit | No | ||
| orphaCode | Yes |
find_diseases_by_phenotypesBuscar doenças por fenótiposInspect
Match por IDs HPO. Use para diagnóstico diferencial.
| Name | Required | Description | Default |
|---|---|---|---|
| limit | No | ||
| hpo_ids | Yes |
find_papers_for_diseasePapers de uma doençaInspect
Literatura relacionada a uma doença via embeddings (:SEMANTIC_MATCH, fallback vetorial).
| Name | Required | Description | Default |
|---|---|---|---|
| limit | No | ||
| min_score | No | ||
| orphaCode | Yes |
find_phenotypically_similarDoenças com fenótipos similaresRead-onlyInspect
Doenças com perfil de fenótipos HPO semelhante (simGIC pré-computado, explicável: nº de fenótipos em comum). Complementa find_similar_diseases (semântico).
| Name | Required | Description | Default |
|---|---|---|---|
| limit | No | ||
| orphaCode | Yes |
Output Schema
| Name | Required | Description |
|---|---|---|
| method | Yes | |
| results | Yes | |
| orphaCode | Yes |
find_reference_centersCentros de referênciaInspect
Centros por doença e/ou UF, com CNES.
| Name | Required | Description | Default |
|---|---|---|---|
| limit | No | ||
| state | No | ||
| orphaCode | No |
find_similar_diseasesDoenças similaresInspect
Vector similarity via embeddings SOTA.
| Name | Required | Description | Default |
|---|---|---|---|
| limit | No | ||
| orphaCode | Yes |
get_disease_detailDetalhes de doença raraInspect
Fenótipos HPO, genes, SUS, trials, descrição clínica em PT.
| Name | Required | Description | Default |
|---|---|---|---|
| orphaCode | Yes |
get_evidenceProveniência / evidênciasRead-onlyInspect
Cross-references de autoridade (Orphanet, MONDO, OMIM, MeSH, GARD, UMLS), status de verificação e PMIDs de uma doença. A base da regra "nunca inventar".
| Name | Required | Description | Default |
|---|---|---|---|
| orphaCode | Yes |
Output Schema
| Name | Required | Description |
|---|---|---|
| name | Yes | |
| pmids | Yes | |
| xrefs | Yes | |
| orphaCode | Yes | |
| diseaseTwin | Yes | |
| neverInvent | Yes | |
| verification | Yes |
get_graph_statsEstatísticas do grafoInspect
Contagens e métricas do dataset.
| Name | Required | Description | Default |
|---|---|---|---|
No parameters | |||
get_hypothesesHipóteses de reposicionamento (co-scientist)Read-onlyInspect
Candidatos a reposicionamento de fármacos gerados por associação de genes (guilt-by-association): drogas que tratam outras doenças que compartilham genes com esta. HIPÓTESES para investigação, NUNCA recomendações clínicas — cada uma rastreável (via gene X, da doença Y).
| Name | Required | Description | Default |
|---|---|---|---|
| orphaCode | Yes |
Output Schema
| Name | Required | Description |
|---|---|---|
| name | Yes | |
| method | Yes | |
| orphaCode | Yes | |
| hypotheses | Yes | |
| isRecommendation | Yes |
get_literature_relationsRelações mineradas da literatura (PubTator3)Read-onlyInspect
Relações tipadas extraídas da literatura biomédica (associate/treat/cause/inhibit/stimulate/prevent) entre a doença e genes/fármacos, com nº de publicações como proveniência. Filtrável por predicado.
| Name | Required | Description | Default |
|---|---|---|---|
| orphaCode | Yes | ||
| predicate | No |
Output Schema
| Name | Required | Description |
|---|---|---|
| source | Yes | |
| orphaCode | Yes | |
| relations | Yes |
get_recent_updatesDisease Twins atualizados recentementeRead-onlyInspect
Doenças cujo gêmeo digital ganhou evidência nova (autoria, PubTator3, Open Targets, verificação) nos últimos N dias. Faça polling para acompanhar mudanças (substituto stateless de subscriptions).
| Name | Required | Description | Default |
|---|---|---|---|
| days | No | ||
| limit | No |
Output Schema
| Name | Required | Description |
|---|---|---|
| updates | Yes | |
| sinceDays | Yes |
get_research_logDiário de pesquisa do Disease TwinRead-onlyInspect
Registro cronológico do que o agente autônomo fez por esta doença: autoria, mineração de literatura, evidência genética, verificação, prospecção de fontes, recomputação de relações. Prova de que o gêmeo digital estuda a doença continuamente.
| Name | Required | Description | Default |
|---|---|---|---|
| orphaCode | Yes |
Output Schema
| Name | Required | Description |
|---|---|---|
| name | Yes | |
| events | Yes | |
| orphaCode | Yes |
get_schemaEsquema do grafoRead-onlyInspect
Node labels, relationship types e property keys do grafo. Use antes de cypher_query.
| Name | Required | Description | Default |
|---|---|---|---|
No parameters | |||
get_sus_coverageCobertura SUSInspect
CEAF, SIGTAP, PNTN, nível de integração.
| Name | Required | Description | Default |
|---|---|---|---|
| orphaCode | Yes |
search_diseasesBuscar doenças rarasInspect
Full-text search em 10.468 doenças raras. Suporta filtros SUS/trials.
| Name | Required | Description | Default |
|---|---|---|---|
| limit | No | ||
| query | Yes | ||
| filter_has_sus_coverage | No | ||
| filter_has_active_trials | No |
search_papers_semanticBusca semântica de papersInspect
Busca vetorial sobre 424k papers do PubMed. Use caso clínico, pergunta ou conjunto de sintomas.
| Name | Required | Description | Default |
|---|---|---|---|
| limit | No | ||
| query | Yes | ||
| min_score | No |
search_phenotypesBuscar fenótipos HPOInspect
Lookup HPO em PT ou EN. Retorna IDs HP:.
| Name | Required | Description | Default |
|---|---|---|---|
| limit | No | ||
| query | Yes |
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