Rare disease auxiliary diagnosis method and system

• Main Authors: HUANG SHUXIN, XIE WENLONG, CHEN RONGSHAN, CHEN ZHANNI, ZENG YUANHUAN, WANG LIN, GUO LISHA, XIONG HUI, ZHANG FENGFENG, LIAO XIAOJIA, YAO XUN
• Format: Patent
• Language: Chinese; English
• Published: 26.01.2021
• Subjects: HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATIONTECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING ORPROCESSING OF MEDICAL OR HEALTHCARE DATA; INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTEDFOR SPECIFIC APPLICATION FIELDS; PHYSICS

The invention provides a method and a system for guiding a rare patient to see a doctor, which can provide real-time doctor-seeing suggestions for the rare patient by analyzing clinical symptom information, including possibly related rare disease information corresponding to a clinical symptom. And disease description, phenotype of a disease affected system, and information such as a first diagnosis department, a treatment process, an examination subject, a confirmed key clinical indication, an examination means and the like of the disease are described. Rare patients do not need to purposively run around to seek medical advice any more, the diagnosis time of the rare diseases is greatly shortened, the best treatment opportunity is won for the patients, and meanwhile, the economic and mental burdens of patient families are also reduced. 本发明提供了一种用于指导罕见病患者就诊的方法及系统，能通过对临床症状信息的分析，为罕见病患者提供实时的就诊建议，包括临床症状对应的可能相关的罕见病信息，疾病描述、疾病受累系统的表型以及疾病的首诊科室、就诊流程、检查科目、确诊的关键临床指征及检查手段等信息。让罕见病患者不再毫无目的性的四处奔波求医，大大缩短了罕见病的诊断时间，为患者赢得最佳治疗时机，