{"skill":{"slug":"rare-disease-hpo-mapper","displayName":"Rare Disease HPO Mapper","summary":"Map patient symptoms to Human Phenotype Ontology terms for gene diagnosis.","tags":{"latest":"1.0.0"},"stats":{"comments":0,"downloads":119,"installsAllTime":0,"installsCurrent":0,"stars":0,"versions":1},"createdAt":1774929506278,"updatedAt":1774930008322},"latestVersion":{"version":"1.0.0","createdAt":1774929506278,"changelog":"Initial release of rare-disease-hpo-mapper.\n\n- Maps patient symptoms to Human Phenotype Ontology (HPO) terms for gene diagnosis.\n- Provides a structured workflow for input validation, reproducible outputs, and error handling.\n- Includes example usage, audit-ready commands, and parameter definitions.\n- Offers risk assessment, security checklist, and explicit output requirements.\n- Supports use cases such as rare disease diagnosis, cohort building, and genetic counseling.","license":"MIT-0"},"metadata":null,"owner":{"handle":"aipoch-ai","userId":"s17fjw78yq6wtd4ep6zsaxwrn983hznr","displayName":"AIpoch","image":"https://avatars.githubusercontent.com/u/258999481?v=4"},"moderation":null}