Website that provides a physician/health care provider with useful information about the utility of a family history in identifying disease risk and developing a personalized prevention program. Family history questionnaires to use when gathering a complete and accurate family medical history. Family history readings to assist providers in diagnosis of disease risk.
| Type | Other, Website |
| CME Available | No |
| Topic | Genetic Counseling |
| Cost | |
| Note | Website and family history forms available for download. |
Genomic Competencies
Experts from the disciplines listed below have tagged this resource as fulfulling genomic competencies.
Nurse
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Collect a patient’s personal and three generation family health history to assess for genomic factors that impact the patient’s health.
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Discuss the ways in which nurses can meet the educational, psychosocial and resource needs of patients and families affected by a genetic or genomic condition.
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Identification
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ID-1: Identify clients who may benefit from genetic and genomic information and services
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ID1-K4: Common health conditions with a genetic/genomic component
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ID1-2: Identify clients who may benefit from further evaluation of the identified disease susceptibility or genetic/genomic condition.
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ID1-1: Identify factors in a family and health history that contribute to: disease susceptibility; disease characteristics, treatment, prognosis; or genetic/genomic condition.
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ID1-4: Uses genetic and genomic indicators as rationale for clients who may benefit from further evaluation or other risk management interventions.
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ID1-K1: Components of family history needed to identify disease susceptibility or genetic/genomic condition
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ID1-2: Identify clients who may benefit from further evaluation of the identified disease susceptibility or genetic/genomic condition.
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ID1-1: Identify factors in a family and health history that contribute to: disease susceptibility; disease characteristics, treatment, prognosis; or genetic/genomic condition.
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ID1-4: Uses genetic and genomic indicators as rationale for clients who may benefit from further evaluation or other risk management interventions.
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ID1-K3: Indicators of disease susceptibility or a genetic condition
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ID1-2: Identify clients who may benefit from further evaluation of the identified disease susceptibility or genetic/genomic condition.
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ID1-1: Identify factors in a family and health history that contribute to: disease susceptibility; disease characteristics, treatment, prognosis; or genetic/genomic condition.
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ID1-4: Uses genetic and genomic indicators as rationale for clients who may benefit from further evaluation or other risk management interventions.
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ID1-K5: Indicators of need for targeted treatment selection
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ID1-2: Identify clients who may benefit from further evaluation of the identified disease susceptibility or genetic/genomic condition.
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ID1-1: Identify factors in a family and health history that contribute to: disease susceptibility; disease characteristics, treatment, prognosis; or genetic/genomic condition.
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ID1-4: Uses genetic and genomic indicators as rationale for clients who may benefit from further evaluation or other risk management interventions.
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ID1-K2: Inheritance patterns
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ID1-2: Identify clients who may benefit from further evaluation of the identified disease susceptibility or genetic/genomic condition.
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ID1-1: Identify factors in a family and health history that contribute to: disease susceptibility; disease characteristics, treatment, prognosis; or genetic/genomic condition.
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ID1-4: Uses genetic and genomic indicators as rationale for clients who may benefit from further evaluation or other risk management interventions.
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ID-2: Identify credible, accurate, appropriate, and current genetic and genomic information
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ID2-K4: Interprofessional resources
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ID2-2: Discuss the ways in which nurses can meet the educational, psychosocial and resource needs of clients and families affected by a genetic or genomic condition.
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ID2-K1: Resources for health care professionals and lay public
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ID2-2: Discuss the ways in which nurses can meet the educational, psychosocial and resource needs of clients and families affected by a genetic or genomic condition.
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ID2-K2: Resources for referral within one’s community
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ID2-2: Discuss the ways in which nurses can meet the educational, psychosocial and resource needs of clients and families affected by a genetic or genomic condition.
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ID2-K3: Roles of genetic/genomic health care professionals
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ID2-2: Discuss the ways in which nurses can meet the educational, psychosocial and resource needs of clients and families affected by a genetic or genomic condition.
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Nursing Assessment
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NA-6: Analyze the history and physical assessment for genetic, environmental, and genomic influences
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NA6-K3: Assessment and diagnosis of acute and chronic disease
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NA6-2: Demonstrate ability to incorporate family history as part of the nursing assessment.
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NA6-3: Document family history information on three-generations on both maternal and paternal side, when available.
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NA6-4: Document key genetic and genomic assessment information.
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NA6-5: Identify components of assessment data that contribute to disease and/or health risks to establish a plan of care.
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NA6-1: Identify genetic and genomic factors within collected history and physical assessment data that contribute to disease and/or health risks.
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NA6-K2: Indicators of disease susceptibility or a genetic condition
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NA6-2: Demonstrate ability to incorporate family history as part of the nursing assessment.
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NA6-3: Document family history information on three-generations on both maternal and paternal side, when available.
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NA6-4: Document key genetic and genomic assessment information.
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NA6-5: Identify components of assessment data that contribute to disease and/or health risks to establish a plan of care.
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NA6-1: Identify genetic and genomic factors within collected history and physical assessment data that contribute to disease and/or health risks.
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NA6-K1: Pathophysiological, medical and nursing evaluation of common acute and chronic disease
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NA6-2: Demonstrate ability to incorporate family history as part of the nursing assessment.
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NA6-3: Document family history information on three-generations on both maternal and paternal side, when available.
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NA6-4: Document key genetic and genomic assessment information.
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NA6-5: Identify components of assessment data that contribute to disease and/or health risks to establish a plan of care.
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NA6-1: Identify genetic and genomic factors within collected history and physical assessment data that contribute to disease and/or health risks.
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NA-4: Collect histories that consider genetic, environmental, and genomic influences and risks
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NA4-K2: Basics of risk factors
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NA4-1: Demonstrate ability to collect personal, medical and family history that includes genetic/genomic as well as environmental risks.
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NA4-K1: Fundamentals of genetic and genomic focused health assessment
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NA4-1: Demonstrate ability to collect personal, medical and family history that includes genetic/genomic as well as environmental risks.
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NA-5: Conducts assessments incorporating genetic, environmental, and genomic influences and risk factors
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NA5-K2: Basics of risk factors
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NA1-7: Incorporate genetic and genomic health assessment data into routinely collected biopsychosocial and environmental assessments of health and illness parameters in client, using culturally sensitive approaches.
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NA5-K1: Fundamentals of genetic and genomic focused health and physical assessment
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NA1-7: Incorporate genetic and genomic health assessment data into routinely collected biopsychosocial and environmental assessments of health and illness parameters in client, using culturally sensitive approaches.
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NA-3: Construct a pedigree from collected family history
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NA3-K1: Components of family history needed to identify disease susceptibility or genetic/genomic condition
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NA2-1: Demonstrate ability to elicit a complete three-generation family health history.
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NA-2: Demonstrate ability to elicit three-generation family health history information
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NA2-K1: Components of family history needed
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NA2-1: Demonstrate ability to elicit a complete three-generation family health history.
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NA2-2: Identify available family history tools to facilitate collection of family health history information.
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NA-1: Demonstrate understanding of relationship of genetics and genomics to health
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NA1-K3: Basic principles of pharmacogenetics and pharmacogenomics
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NA1 – 1: Collect a client’s personal and three generation family health history to assess for genomic factors that impact the client’s health.
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NA1-3: Identify clients who might benefit from referral to genetic specialists and/or information resources.
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NA1-2: Identify potentially significant information from a family history.
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NA1-7: Incorporate genetic and genomic health assessment data into routinely collected biopsychosocial and environmental assessments of health and illness parameters in client, using culturally sensitive approaches.
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NA1-K4: Patterns of disease associated with single gene and multifactorial inheritance
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NA1 – 1: Collect a client’s personal and three generation family health history to assess for genomic factors that impact the client’s health.
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NA1-3: Identify clients who might benefit from referral to genetic specialists and/or information resources.
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NA1-2: Identify potentially significant information from a family history.
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NA1-K1: Relationship of genetics and genomics to health
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NA1 – 1: Collect a client’s personal and three generation family health history to assess for genomic factors that impact the client’s health.
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NA1-3: Identify clients who might benefit from referral to genetic specialists and/or information resources.
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NA1-2: Identify potentially significant information from a family history.
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NA1-7: Incorporate genetic and genomic health assessment data into routinely collected biopsychosocial and environmental assessments of health and illness parameters in client, using culturally sensitive approaches.
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NA1-K2: Relationship of genetics and genomics to normal physiology and pathophysiology
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NA1 – 1: Collect a client’s personal and three generation family health history to assess for genomic factors that impact the client’s health.
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NA1-3: Identify clients who might benefit from referral to genetic specialists and/or information resources.
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NA1-2: Identify potentially significant information from a family history.
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NA1-7: Incorporate genetic and genomic health assessment data into routinely collected biopsychosocial and environmental assessments of health and illness parameters in client, using culturally sensitive approaches.
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Provision of education, care and support
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PECS-1: Provide clients with interpretation of genetic and genomic information
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PECS1-K1: Components of family history
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PECS1-2: Use family history information to inform health education.
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PECS1-K4: Informed consent procedures and essential elements
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PECS1-2: Use family history information to inform health education.
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PECS1-K2: Inheritance Patterns
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PECS1-2: Use family history information to inform health education.
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PECS1-K3: Role of environmental and psychosocial factors
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PECS1-2: Use family history information to inform health education.
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PECS-3b: Use health promotion/disease prevention practices incorporating knowledge of genetic and/or genomic risk factors
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NA1-7: Incorporate genetic and genomic health assessment data into routinely collected biopsychosocial and environmental assessments of health and illness parameters in client, using culturally sensitive approaches.
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PECS-3a: Use health promotion/disease prevention practices that consider genetic and genomic influences
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PECS3-K2: Fundamentals of epidemiology and biostatistics
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NA1-7: Incorporate genetic and genomic health assessment data into routinely collected biopsychosocial and environmental assessments of health and illness parameters in client, using culturally sensitive approaches.
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PECS3-K3: Ongoing research contributing to improved understanding of the genetic/genomic influences on health
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NA1-7: Incorporate genetic and genomic health assessment data into routinely collected biopsychosocial and environmental assessments of health and illness parameters in client, using culturally sensitive approaches.
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PECS3-K1: Role of environmental and psychosocial factors
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NA1-7: Incorporate genetic and genomic health assessment data into routinely collected biopsychosocial and environmental assessments of health and illness parameters in client, using culturally sensitive approaches.
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Uses genetic and genomic indicators as rationale for patients who may benefit from further evaluation or other risk management interventions.