公开(公告)号：US10910108B2

公开(公告)日：2021-02-02

申请号：US15393817

申请日：2016-12-29

Applicant: CERNER INNOVATION, INC.

Inventor： Soumen Tapadar ,  Leena Verma

IPC: G06F21/62 ,  G06Q50/00 ,  G16H50/30 ,  G16H50/20 ,  G16H10/60 ,  G16H40/67 ,  G16H40/63

Abstract: Systems, methods and computer-readable media are provided for identification of patients or family member having genetic disease or probable genetic disease. During or after registration of a patient, parents, grandparents, or siblings of the patient are identified. If it is determined that one of the patient or the parents, grandparents, or siblings of the patient has been assigned with a diagnosis indicating a genetic disease, an alert for genetic disease or probable genetic disease for the patient or family member of the patient is provided. A clinician is then prompted to confirm or rule out the patient or family member inheriting the disease.

公开(公告)号：US20230402188A1

公开(公告)日：2023-12-14

申请号：US18457692

申请日：2023-08-29

Applicant: Cerner Innovation, Inc.

Inventor： Soumen Tapadar ,  Leena Verma

IPC: G16H50/30 ,  G16H50/20 ,  G16H10/60 ,  G16H40/67 ,  G16H40/63

CPC classification number: G16H50/30 ,  G16H50/20 ,  G16H10/60 ,  G16H40/67 ,  G16H40/63

Abstract: Systems, methods and computer-readable media are provided for identification of patients or family member having genetic disease or probable genetic disease. During or after registration of a patient, parents, grandparents, or siblings of the patient are identified. If it is determined that one of the patient or the parents, grandparents, or siblings of the patient has been assigned with a diagnosis indicating a genetic disease, an alert for genetic disease or probable genetic disease for the patient or family member of the patient is provided. A clinician is then prompted to confirm or rule out the patient or family member inheriting the disease.

公开(公告)号：US11776695B2

公开(公告)日：2023-10-03

申请号：US17154259

申请日：2021-01-21

Applicant: CERNER INNOVATION, INC.

Inventor： Soumen Tapadar ,  Leena Verma

IPC: G16H50/30 ,  G16H50/20 ,  G16H10/60 ,  G16H40/67 ,  G16H40/63

CPC classification number: G16H50/30 ,  G16H10/60 ,  G16H40/63 ,  G16H40/67 ,  G16H50/20

Abstract: Systems, methods and computer-readable media are provided for identification of patients or family member having genetic disease or probable genetic disease. During or after registration of a patient, parents, grandparents, or siblings of the patient are identified. If it is determined that one of the patient or the parents, grandparents, or siblings of the patient has been assigned with a diagnosis indicating a genetic disease, an alert for genetic disease or probable genetic disease for the patient or family member of the patient is provided. A clinician is then prompted to confirm or rule out the patient or family member inheriting the disease.