Electronic medical records system utilizing genetic information

1. A method comprising:

receiving data, the data identifying medical information;

determining, by a processor, an internal medical code associated with the medical information, the internal medical code being a non-genetic code, the internal medical code being machine readable and independent of genetic information;

determining, by a processor, genetic variants associated with the internal medical code, the determined genetic variant comprising a chromosome, the determined genetic variant being determined from a first database storing data identifying a plurality of genetic variants;

generating, by a processor, a graphical user interface, the graphical user interface displaying at least one of the determined genetic variants, the identity of a gene, and a location of the gene within the chromosome, the graphical user interface comprising a selectable link connecting the displayed genetic variant to further information associated with the displayed genetic variant;

presenting the genetic variants in a graphical format using a computing device; and

upon selecting the selectable link:

retrieving data over the Internet from a second database, the data related to the gene; and

modifying the graphical user interface to present the further information associated with the displayed genetic variant.

2. The method of claim 1 , further comprising:

determining a relevance score associated with the internal medical code and each of the genetic variants;

filtering the genetic variants based on the relevance score; and

presenting a filtered group of the genetic variants in a graphical format using the computing device.

3. The method of claim 1 , wherein the graphical format displays one or more genes associated with the genetic variants and locations of the one or more genes on associated chromosomes.

4. The method of claim 3 , wherein a user is enabled to select the one or more genes to view more information about the one or more genes.

5. A method comprising:

receiving data from a first database, the data identifying genetic information;

determining, by a processor, an internal medical code associated with the genetic information, the internal medical code being a non-genetic code, the internal medical code being machine readable and independent of the genetic information:

determining, by a processor, medical findings associated with the internal medical code;

generating, by a processor, a graphical user interface, the graphical user interface displaying the genetic information, the graphical user interface comprising a selectable link connecting the displayed genetic information to the determined medical findings; and

upon selecting the selectable control:

retrieving data from a second database remotely, the second database remote from the first database, the data related to the medical findings; and

presenting the medical findings in a list format using the computing device upon actuating the selectable link.

6. The method of claim 5 , further comprising:

determining a relevance score associated with the internal medical code and each of the medical findings:

filtering the medical findings based on the relevance score; and

presenting a filtered group of the medical findings in a list format using the computing device.

7. The method of claim 5 , wherein the list format enables a user to select one of the medical findings to view information about a selected medical finding.

8. The method of claim 7 , wherein the information includes whether a patient medical record includes an instance of the selected medical finding.

9. A method comprising:

receiving an input;

determining, by a processor, an internal medical code associated with the input, the internal medical code being a non-genetic code;

determining, by a processor, microbiome genetic information associated with the internal medical code, wherein the microbiome genetic information is associated with genes of microorganisms living within a person which are related to the input, the determined microbiome being identified from a first database;

generating, by a processor, a graphical user interface, the graphical user interface displaying the microbiome genetic information, the graphical user interface comprising a selectable link connecting the input to the determined medical findings; and

upon selecting the selectable link, presenting the microbiome genetic information in a graphical format using a computing device upon actuating the selectable link,

the internal medical code being machine readable and independent of the genetic information.

10. The method of claim 9 , wherein the graphical format indicates a microorganism associated with the microbiome genetic information.

11. The method of claim 9 , wherein the microbiome genetic information indicates the presence or absence of a microorganism.

12. The method of claim 9 further comprising:

receiving a human genetic variant;

determining an internal medical code associated with the human genetic variant;

determining medical items associated with the internal medical code; and

presenting the medical items in a list format on the computing device, wherein the input is at least one of the medical items.

13. A system comprising:

a database encoded on a memory device, the database having a library, the library including medical findings, genetic information, and one or more patient medical records;

a computing device in data communication with the database, wherein the computing device is programmed to:

receive an input;

determine an internal medical code associated with the input, the internal medical code being a non-genetic code;

determine related genetic variants associated with the internal medical code, the related genetic variants selected from the genetic information in the library, the determined genetic variants comprising a chromosome, the determined genetic variants being determined from a first database storing data identifying a plurality of genetic variants;

generate a graphical user interface, the graphical user interface displaying at least one of the determined related genetic variants and a gene associated with the displayed related genetic variant, the graphical user interface comprising a selectable link connecting the displayed related genetic variant to further information associated with the displayed related genetic variant;

upon selecting the selectable control, retrieving data over the Internet from a second database, the data related to the gene, and presenting the related genetic variants in a graphical format; and

the internal medical code being machine readable and independent of genetic information.

14. A system comprising:

a database encoded on a memory device, the database having genetic information associated with abnormal medical findings, and one or more patient medical records;

a computing device in data communication with the database, wherein the computing device is programmed to:

access a patient medical record from the one or more patient medical records;

identify tumor sequencing information in the patient medical record, the tumor sequencing information associated with a non-genetic internal medical code, the identified tumor sequencing information being identified from a first database storing tumor sequencing information;

determine related genetic information associated with the tumor sequencing information from the genetic information associated with tumors, the determined related genetic information being associated with the non-genetic internal medical code of the tumor sequencing information, the determined related genetic information being identified from a second database storing genetic information, the second database remote from the first database;

generate a graphical user interface, the graphical user interface displaying the tumor sequencing information, the graphical user interface comprising a selectable link connecting the displayed tumor sequencing information to the related genetic information;

upon selecting the selectable control, retrieving the determined genetic information over the Internet, and presenting the related genetic information in a graphical format; and

the internal medical code being machine readable and independent of genetic information.