Indicator For Probable Inheritance Of Genetic Disease

A method, comprising:

• determining a first update to a first electronic health record corresponding to a first patient;
• determining that the first update comprises a first genetic disease indication corresponding to the first patient;
• responsive to determining that the first update comprises the first genetic disease indication corresponding to the first patient:
• determining an association between the first electronic health record corresponding to the first patient and a second electronic health record corresponding to a second patient, wherein the second patient has a familial relationship with the first patient;
• based on (a) the first genetic disease indication and (b) the association between the first electronic health record and the second electronic health record:
• generating a second update comprising a second genetic disease indication corresponding to the second patient;
• applying the second update to the second electronic health record;
• wherein the method is performed by at least one device comprising a hardware processor.

A system, comprising:

• at least one processor;
• and
• wherein the at least one processor is configured to perform operations, comprising:
• determining a first update to a first electronic health record corresponding to a first patient;
• determining that the first update comprises a first genetic disease indication corresponding to the first patient;
• responsive to determining that the first update comprises the first genetic disease indication corresponding to the first patient:
• determining an association between the first electronic health record corresponding to the first patient and a second electronic health record corresponding to a second patient, wherein the second patient has a familial relationship with the first patient;
• based on (a) the first genetic disease indication and (b) the association between the first electronic health record and the second electronic health record:
• generating a second update comprising a second genetic disease indication corresponding to the second patient;
• applying the second update to the second electronic health record.