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Any disease which can be self-reported could be a candidate for crowdsourcing. For example, the National Databank of Rheumatic diseases crowdsources their enrollment and follow up on a variety of rheumatic diseases, some of which are uncommon. They are able to gather valuable self-reported function and quality of life information through longitudinal surveys. An online portal makes good sense for rare diseases which don't have an established national network. The National Organization of Rare diseases uses crowdsourced portals for rare disease registries. Jonathan Haidt has done fascinating and valuable psychological research through ongoing crowdsourced surveys such as The potential of crowdsourcing medical research is just beginning to be tapped.

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