orphadata.raredisease.disease_natural_history
shallowio.github.whiteknightonhorse/apibase · Verify this server
Get genetic inheritance mode and clinical timeline for a rare disease by its Orphanet ORPHAcode. Returns inheritance modes (e.g. Autosomal dominant, X-linked recessive, Mitochondrial), average age of onset (e.g. Neonatal, Infancy, All ages), and disease group/typology classification. Supports 12 languages (en, fr, de, es, it, pt, nl, pl, cs, tr, uk, zh). Source: Orphadata / Orphanet — CC BY 4.0, no auth, unlimited free.
1 trials · measured 14 days ago
orphadata.raredisease.disease_natural_history scores 100.0/100 on Vouch's measured behaviour index, from 1 real invocation trials against io.github.whiteknightonhorse/apibase, measured 23 Sept 2026 under methodology v0.2.0. Every measured component scored 100.
Component breakdown
| Component | Weight | Value |
|---|---|---|
| Reliability | 35% | not applicable |
| Schema integrity | 25% | 100.0 |
| Failure behaviour | 15% | not applicable |
| Latency | 15% | not applicable |
| Concurrency | 10% | not applicable |
Tool details
- Transport
- remote + stdio
- Credential class
- self-provisionable
- Input schema
- not declared
- Output schema
- not declared
- Side-effect classification
- unclassified
Score history
| Day | Score | Tier | Methodology |
|---|---|---|---|
| 2026-09-23 | 100.0 | shallow | v0.2.0 |
Probe evidence
| Probe | Outcomes |
|---|---|
| schema_integrity | pass: 1 |
Raw request/response logs are not archived yet — the outcome counts above are drawn directly from every recorded trial.
Embed this score
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[](https://vouch.tools/tools/ffda21c1-0ecc-4f3a-a1c5-f45990c727f1)