Indicator For Probable Inheritance Of Genetic Disease

The media of claim 1, wherein the operations further comprise:

• responsive to determining the first diagnosis of the first patient:
• transmitting a communication to a medical device associated with the second patient;
• and
• receiving a fourth medical record from the medical device, wherein the fourth medical record comprises an insight as to whether the second patient is diagnosable with the second diagnosis.

The media of claim 1, wherein the operations further comprise:

• receiving, by the genetic disease engine, one or more electronic health records associated with a registration of the first patient in the healthcare system;
• identifying, by the genetic disease engine, the second patient in the healthcare system, wherein the second patient is registered in the healthcare system;
• and
• generating, by the genetic disease engine, a relationship between the first patient and the second patient in the healthcare system.

A method, comprising:

• determining, by a genetic disease engine, a first diagnosis of a first patient in a first electronic health record associated with the first patient, wherein the first diagnosis is made by a first clinician, and wherein the first diagnosis indicates a genetic disease or a probable genetic disease;
• responsive to determining the first diagnosis of the first patient:
• identifying, by the genetic disease engine, a second electronic health record in a healthcare system, wherein the second electronic health record comprises an identification of a second patient as a family member of the first patient;
• generating, by the genetic disease engine, a third electronic health record in the healthcare system, wherein the third electronic health record comprises an order that assists a second clinician in determining whether the second patient is diagnosable with a second diagnosis or in providing treatment with respect to the second diagnosis, wherein the second diagnosis comprises the genetic disease or the probable genetic disease;
• transmitting for display on a clinician device, a prompt indicative of the third electronic health record comprising the order having been generated in the healthcare system, wherein the third electronic health record comprising the order is accessed via the clinician device.

A system, comprising:

• a genetic disease engine comprising at least one processor;
• and
• wherein the genetic disease engine is configured to perform operations, comprising:
• determining a first diagnosis of a first patient in a first electronic health record associated with the first patient, wherein the first diagnosis is made by a first clinician, and wherein the first diagnosis indicates a genetic disease or a probable genetic disease;
• responsive to determining the first diagnosis of the first patient:
• identifying a second electronic health record in a healthcare system, wherein the second electronic health record comprises an identification of a second patient as a family member of the first patient;
• generating a third electronic health record in the healthcare system, wherein the third electronic health record comprises an order that assists a second clinician in determining whether the second patient is diagnosable with a second diagnosis or in providing treatment with respect to the second diagnosis, wherein the second diagnosis comprises the genetic disease or the probable genetic disease;
• transmitting for display on a clinician device, a prompt indicative of the third electronic health record comprising the order having been generated in the healthcare system, wherein the third electronic health record comprising the order is accessed via the clinician device.