Rare Disease Identification

The Rare Disease Identification is the first step in a medical diagnosis of a genetic disorder. The application categorizes several, recognizable and common genetic symptoms so that consumers can identify and select symptoms they observe in their family. With the identification of more symptoms and features, consumers will have a clearer idea that their family members have a genetic disorder and can report these symptoms to local hospitals and doctors. Hopefully, the lives of several patients are improved through early diagnosis of the disease.