Systems and Methods for Diagnosing Inherited Retinal Diseases

A computer device for automatically diagnosing inherited retinal disease, the computer device comprising:

• one or more processors;
• and
• one or more memories coupled to the one or more processors;
• wherein the one or more memories include computer executable instructions stored therein that, when executed by the one or more processors, cause the one or more processors to:
• receive, via a network interface, a plurality of dissimilar types of data from an end user device, the plurality of dissimilar types of data being related to retinal disease and the plurality of dissimilar types of data corresponding to a patient;
• pre-process at least one of the plurality of dissimilar types of data to generate a feature vector descriptive of the patient;
• for each of the plurality of dissimilar types of data:
• compare portions of the respective type of data or a corresponding feature vector to data in a mutation proven database, wherein the data in the mutation proven database is similar to the respective type of data and wherein the data in the mutation proven database corresponds to a plurality of patients with known diagnoses,
• generate a ranked list of matches between the patient and the plurality of patients with known diagnoses, and
• store the ranked list of matches in an output database,
• aggregate a plurality of ranked lists of matches in the output database to generate a ranked list of genetic diagnoses corresponding to the patient;
• and
• send an indication of the ranked list of genetic diagnoses to the end user device.