Rare disease research group management system, client and server

Abstract

The invention discloses a rare disease research group management system. The system comprises a client and a server which perform data interaction with each other. The client comprises a sending unitused for sending a group creation request and a group joining application approval result to the server; a receiving unit used for receiving a multi-center group auditing result and group joining application information sent by the server; and an approval unit which is in communication connection with the sending unit and the receiving unit and is used for approving the group joining application.The server comprises: a receiving unit, which is used for receiving the group creation request, the group joining application information and the group joining application approval result sent by theclient; a sending unit which is used for sending the multi-center group auditing result, the group joining application information and the group joining application approval result to the client; anda group creation unit which is in communication connection with the receiving unit and the sending unit. According to the invention, researchers researching the same disease can form a group, and intra-group data sharing is realized, so that effective rare disease research can be carried out.

Description

technical field [0001] The present invention relates to the technical field of group management systems, in particular to a rare disease research group management system, client and server. Background technique [0002] Rare diseases are referred to as "rare diseases" for short, also known as "orphan diseases". Most rare diseases are chronic, severe conditions that are often life-threatening. About 80% of rare diseases are caused by genetic defects, so rare diseases generally refer to "rare genetic diseases". According to the report of the World Health Organization (WHO), there are more than 5,000 recognized rare diseases, accounting for about 10% of human diseases; about 50% of rare diseases can occur at birth or in childhood, and the disease often progresses Rapidly, the mortality rate is very high, and most of them still have no effective treatment method, which causes great suffering to the patients. [0003] Rare disease is a relative, dynamic, and changing concept. ...

AI Technical Summary

Problems solved by technology

[0006] In view of this, the purpose of the embodiment of the present invention is to propose a rare disease research group management system, client and server, which can solve the problems that researchers cannot conduct research on rare diseases in the form of group collaborative work and case sharing.

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