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orphadata.raredisease.disease_natural_history

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 ...

SERVERApibase SOURCEapibase-mcp-client
Low RISK CLASS
Category Read
Parameters 21 required
Recommended Allowedsee the rule below
Registry record Grade F, identity unverified Pull the record →

This record as markdown: /tools/io-github-whiteknightonhorse-apibase/orphadata.raredisease.disease-natural-history.md

What orphadata.raredisease.disease_natural_history does on Apibase

AI agents call orphadata.raredisease.disease_natural_history to retrieve information from Apibase without modifying anything. It is typically the context-gathering step in research, monitoring, and reporting workflows, before the agent takes action elsewhere.

ParameterTypeRequiredDescription
lang string — Response language (default: en). Supported: en, fr, de, es, it, pt, nl, pl, cs, tr, uk, zh.
orphacode integer Yes Orphanet ORPHAcode of the rare disease to get inheritance mode and age-of-onset data for (e.g. 558 for Marfan syndrome).

Parameters from the server's own tool schema.

Why orphadata.raredisease.disease_natural_history is rated Low

Tool retrieves medical reference data without side effects, modifications, or external operations.

From the tool's definition Get genetic inheritance mode and clinical timeline for a rare disease by its Orphanet ORPHAcode.

Questions about orphadata.raredisease.disease_natural_history

What does the orphadata.raredisease.disease_natural_history tool do? +

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. It is categorised as a Read tool in the Apibase MCP Server, which means it retrieves data without modifying state.

What parameters does orphadata.raredisease.disease_natural_history accept? +

orphadata.raredisease.disease_natural_history accepts 2 parameters: lang, orphacode. Required: orphacode. The full parameter table on this page comes from the server's own tool schema.

How do I enforce a policy on orphadata.raredisease.disease_natural_history? +

Register the Apibase MCP server in PolicyLayer and add a rule for orphadata.raredisease.disease_natural_history: allow, deny, rate-limit, or require approval. Point your MCP client at the PolicyLayer proxy URL and the rule is enforced on every call, before it reaches Apibase. Nothing to install.

What risk level is orphadata.raredisease.disease_natural_history? +

orphadata.raredisease.disease_natural_history is a Read tool with low risk. Read-only tools are generally safe to allow by default.

Can I rate-limit orphadata.raredisease.disease_natural_history? +

Yes. Add a rate_limit block to the orphadata.raredisease.disease_natural_history rule in your PolicyLayer policy. For example, setting max: 10 and window: 60 limits the tool to 10 calls per minute. Rate limits are tracked per agent session and reset automatically.

How do I block orphadata.raredisease.disease_natural_history completely? +

Set action: deny in the PolicyLayer policy for orphadata.raredisease.disease_natural_history. The AI agent will receive a policy violation error and cannot call the tool. You can also include a reason field to explain why the tool is blocked.

What MCP server provides orphadata.raredisease.disease_natural_history? +

orphadata.raredisease.disease_natural_history is provided by the Apibase MCP server (apibase-mcp-client). PolicyLayer sits as a proxy in front of this server to enforce policies before tool calls reach the server.

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