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Query Orphanet rare-disease data for nomenclature, genes, phenotypes, and epidemiology.
Copy the install command and let the AI configure it · recommended for beginners
No copy-paste install info for "orphanet-link" yet — see the docs or source repo.
Use orphanet-link to query Orphanet data for spinal muscular atrophy and summarize the disease name, aliases, classification, associated genes, and HPO phenotypes.
A structured summary containing nomenclature, classification hierarchy, gene associations, and typical phenotypes.
Use orphanet-link to query cross-references for Fabry disease, list matching external database identifiers, and present them in a table.
A clear table with the disease name and mapped external database identifiers for comparison and citation.
Use orphanet-link to query epidemiology and natural history information for Duchenne muscular dystrophy, then write a concise summary in English suitable for research notes.
A concise research-note summary covering prevalence, onset characteristics, disease progression, and key clinical information.
Query gene-disease validity data and detect consensus or conflicts across assertions.
Query MGI mouse genetics data for markers, mutations, phenotypes, and disease models.
Retrieve disease-related information for fast medical lookup and research.
Query NHS public health data, prescribing records, and organisation information.
Query UniProt data for proteins, sequences, variants, diseases, and related research.
Search and access ENA RNA sequencing datasets with advanced filtering.