TeleMedical Genetics 6-month Professional Program and Practice Blueprint
Major Learning Outcomes
1 End-to-End Telegenetic Care
Master the complete patient journey from triage and consent through test selection, ordering, interpretation, counseling, documentation, and follow-up in a virtual environment.
2 Compliant Telehealth Operations
Implement HIPAA/HITECH Security Rule controls, OSHA-safe remote protocols, OIG fraud-waste-abuse safeguards, payer-compliant coding/billing, and audit-ready documentation systems.
3 Health IT Integration
Configure EHR systems, analytics platforms, and AI tools with proper interoperability (HL7/FHIR), eConsent workflows, eRx capabilities, and laboratory integrations.
4 Clinical Genomics Application
Translate complex genomic findings into actionable clinical plans across specialties including pharmacogenomics, hereditary cancers, cardiogenetics, metabolic disorders, and reproductive/prenatal genetics.
5 Patient-Centered Service Design
Develop culturally sensitive, equitable telegenetic services that incorporate evidence-based lifestyle medicine and holistic approaches to patient care.
6 Business Development
Create sustainable business models with strategic pricing, payer contracting, efficient patient acquisition, operations dashboards, quality improvement protocols, and comprehensive risk management.
6-Month Curriculum Overview
The program consists of 120 carefully sequenced learning modules delivered over 24 weeks, beginning with orientation and foundations and progressing through specialized clinical applications, compliance frameworks, technology implementation, and business development.
▶ Weeks 2-3: Telehealth Basics and Genetics Fundamentals
Clinical Workflows in Telehealth
Master the essential components of virtual care delivery, including appointment scheduling, documentation, and follow-up protocols.
Patient Selection and Digital Inclusion
Identify appropriate candidates for telegenetics services while addressing technology barriers and accessibility needs.
Tele-triage and Red-flag Escalation
Develop systems to appropriately screen patients and recognize situations requiring urgent in-person assessment.
Tele-consent and Documentation
Implement legally sound electronic consent processes and documentation practices for virtual genetic services.
Managing Emergencies Remotely
Establish protocols for handling clinical emergencies and maintaining duty-of-care in telehealth settings.
Mendelian Inheritance and Penetrance
Review classic inheritance patterns and the concept of variable penetrance in genetic conditions.
Polygenic Risk and Complex Traits
Explore multifactorial inheritance and the clinical application of polygenic risk scores.
Gene-Environment Interactions
Understand how environmental factors influence gene expression through epigenetic mechanisms.
Variant Types and Mechanisms
Classify genetic variants and their potential functional impacts on protein synthesis and function.
Population Genetics Considerations
Apply principles of population genetics and ancestry in test selection and interpretation.
▶ Weeks 4-6: Advanced Genetics and Testing Modalities
Building on the foundation established in Week 3, participants will develop practical skills in family history assessment, hereditary risk identification, and complex genetic concepts including genotype-phenotype correlations and variant of uncertain significance (VUS) management. Cultural competency and effective risk communication strategies round out this critical module.
- Family History & Pedigree Building: Techniques for collecting and documenting 3-4 generation family histories
- Hereditary Red Flags: Identifying patterns suggestive of genetic conditions
- Genotype-Phenotype Correlations: Understanding relationships between genetic variants and clinical presentations
- Genetic Heterogeneity & VUS Management: Approaches to cases with unclear genetic findings
- Cultural Humility & Risk Communication: Culturally sensitive approaches to discussing genetic risk
Cytogenetic & Microarray Analysis
Karyotype, FISH, and chromosomal microarray techniques for detecting large structural variants and copy number changes.
Targeted & Panel Testing
Single-gene analysis and multi-gene panels for specific clinical indications, with considerations for test selection.
Comprehensive Genomic Analysis
Whole-exome sequencing (WES) and whole-genome sequencing (WGS) applications, benefits, and limitations.
Pharmacogenomics & Specialty Testing
PGx testing for medication response, tumor profiling, carrier screening, prenatal testing, and newborn screening protocols.
By the end of Week 6, participants will have developed comprehensive knowledge of genetic testing modalities, their clinical applications, and appropriate test selection criteria for various patient scenarios.
▶ Weeks 7-9: Laboratory Operations and Clinical Skills
Understanding the laboratory side of genetic testing is crucial for telegenetics providers. This module covers regulatory requirements, sample logistics for at-home collection, specimen handling protocols, turnaround time expectations, and report interpretation. Key topics include:
- CLIA/CAP laboratory accreditation standards and requirements
- Remote sample collection logistics for saliva and buccal specimens
- Chain of custody protocols and specimen stability considerations
- Service-level agreements and turnaround time management
- Laboratory report structure and identification of critical values
Accurate variant interpretation is the cornerstone of genetic counseling. Participants will learn standardized classification frameworks, database utilization, computational tools, and literature evaluation methods to assess genetic variants. The module also covers reclassification policies and patient recontacting procedures when variant interpretations change over time.
Week 9: Genetic Counseling SkillsTranslating complex genetic information into understandable guidance requires specialized communication skills. This week focuses on virtual counseling techniques, from pretest education through results delivery, with emphasis on psychosocial assessment, family communication, and accessibility considerations for diverse patient populations.
▶ Weeks 10-12: Clinical Specialties in Genetics
Week 10: Hereditary Cancer Genetics
Cancer genetic testing indications
NCCN-aligned panel selection
Risk management counseling
Virtual tumor boards and second opinions
Survivorship and fertility considerations
Week 11: Cardiogenetics
Channelopathies (LQTS, Brugada, CPVT)
Cardiomyopathies (HCM, DCM, ARVC)
Aortopathies and connective tissue disorders
Familial hypercholesterolemia
Remote monitoring for cardiac phenotyping
Week 12: Neurogenetics and Metabolic Disorders
Epilepsies and neurodevelopmental syndromes
Movement disorders (Huntington, dystonia)
Neuromuscular disorders (DMD/SMA/CMT)
Inborn errors of metabolism
Newborn screening follow-up models
These specialty-focused modules provide in-depth exploration of genetic testing and management across major clinical domains. Each module includes:
- Evidence-Based Guidelines
Current practice standards from professional organizations like NCCN, ACMG, and specialty societies guide clinical decision-making. - Test Selection Criteria
Detailed frameworks for choosing appropriate genetic testing based on family history, personal medical history, and clinical presentation. - Risk Assessment Models
Validated tools for quantifying genetic risk and determining testing thresholds across different clinical scenarios. - Management Protocols
Condition-specific surveillance and intervention recommendations based on genetic test results and clinical context. - Virtual Care Considerations
Special adaptations required for telehealth delivery of these specialized genetic services, including coordination with local providers.
▶ Weeks 13-15: Reproductive Genetics and Pharmacogenomics
1 Week 13: Reproductive and Prenatal Genetics
Master the complexities of genetic counseling throughout the reproductive journey, from preconception carrier screening through pregnancy management and loss evaluation.
Preconception counseling and carrier matching protocols
Distinguishing between screening and diagnostic prenatal tests
Teratogen risk assessment and resource utilization
Genetic evaluation of pregnancy loss
Ethical frameworks for prenatal decision-making discussions
2 Week 14: Pediatric and Adult Rare Disease
Develop expertise in comprehensive genetic evaluation strategies for undiagnosed and rare conditions across the lifespan.
Implementing exome-first diagnostic approaches
Coordinating trio testing workflows for pediatric cases
Establishing virtual undiagnosed disease review boards
Facilitating care coordination with subspecialists
Managing transition from pediatric to adult genetic services
3 Week 15: Pharmacogenomics in Practice
Integrate personalized medication management based on genetic variants affecting drug metabolism and response.
Applying CPIC guidelines for clinical implementation
Interpreting key gene-drug interactions (CYP2D6, CYP2C19, SLCO1B1, HLA)
Configuring EHR clinical decision support alerts
Specialty applications in psychiatry, cardiology, oncology, and pain management
Navigating PGx panel selection and insurance coverage challenges
These specialized modules address complex areas of genetic medicine that require integration with multiple clinical specialties. Participants will learn to:
- Navigate sensitive patient discussions around reproductive choices and rare disease diagnoses
- Develop collaborative care models with maternal-fetal medicine, pediatrics, neurology, and pharmacy
- Create patient-friendly educational materials for complex genetic concepts
- Implement telehealth workflows that accommodate the unique needs of these patient populations
- Establish appropriate documentation and billing practices for these specialized services
▶ Weeks 16-18: Precision Oncology and Regulatory Compliance
Germline vs. Somatic Testing
Understanding the distinct implications of inherited versus tumor-specific genetic alterations and appropriate testing strategies for each.
Tumor-Agnostic Biomarkers
Implementing testing for actionable biomarkers that guide treatment regardless of cancer type, such as MSI-high status and NTRK fusions.
Virtual Molecular Tumor Boards
Establishing and participating in multidisciplinary discussions of complex cancer genomic findings via telehealth platforms.
Clinical Trial Matching
Developing systems to identify appropriate precision oncology trials based on genomic findings and facilitate referrals.
Companion Diagnostics
Navigating FDA-approved companion diagnostic testing requirements for targeted therapies and associated insurance authorization processes.
HIPAA/HITECH/Health IT (Week 17)
HIPAA Privacy Rule implementation in telehealth
Security Rule safeguards (administrative, physical, technical)
HITECH breach notification procedures and BAAs
ONC Cures Act Information Blocking compliance
State-specific privacy requirements and 42 CFR Part 2
OIG/OSHA and Billing Integrity (Week 18)
Telehealth-specific fraud, waste, and abuse risk areas
Stark Law and Anti-Kickback Statute applications
OSHA compliance for remote and small-office settings
Documentation standards for telehealth billing
Audit preparation and incident response protocols
▶ Week 19: Health IT Stack and Interoperability
EHR System
Central patient records and FHIR engine
Telehealth Platform
Video visits and session data exchange
Laboratory Interfaces
Order/results via HL7/FHIR feeds
eConsent & Secure Messaging
Consent capture and encrypted messaging
Analytics Dashboard
Population insights from integrated data
A robust, integrated technology stack is the backbone of any successful telegenetics practice. Week 19 focuses on selecting and implementing the right digital tools to support clinical operations, ensure data security, and enhance patient experience.
EHR Selection for Telegenetics
Evaluate electronic health record systems based on genetics-specific functionality, telehealth integration capabilities, template customization, and cost-effectiveness for small to mid-sized practices.
Laboratory Interfaces and Standards
Implement FHIR/HL7 interfaces for seamless lab order and results transmission, with proper LOINC/SNOMED coding to ensure structured genetic data capture and interoperability.
Digital Patient Engagement Tools
Deploy integrated solutions for electronic consent, identity verification, electronic signatures, family history collection, and secure pre-visit questionnaires to streamline workflow.
Secure Communication Infrastructure
Establish HIPAA-compliant video conferencing, messaging, and data storage systems with appropriate access controls, encryption, and audit capabilities.
Analytics and Quality Measurement
Configure dashboards to track key performance indicators, patient outcomes, and quality metrics specific to telegenetics services for continuous improvement.
- Conducting technology needs assessments based on practice size and specialty focus
- Managing vendor selection and contract negotiation processes
- Creating implementation timelines and staff training plans
- Establishing policies for technology maintenance and updates
- Developing contingency plans for technology failures during patient care
This module provides hands-on experience with sample platforms through lab exercises, allowing participants to practice configuring telehealth systems, EHR templates, and laboratory interfaces in a safe environment before implementing in their own practices.
▶ Weeks 20-22: Practice Management and Business Development
This module covers the foundational elements of establishing a telegenetics practice, including legal structure, licensing considerations for interstate practice, credentialing processes, and operational workflows.
- Entity Formation and Licensure
Selecting appropriate business structures and navigating multistate licensing requirements and interstate compacts. - Credentialing and Enrollment
Streamlining provider credentialing, payer enrollment, and CAQH profile management for telehealth services. - Service Pricing Models
Developing cash-pay options, payer fee schedules, and bundled service packages with competitive market positioning. - Scheduling Optimization
Creating efficient appointment templates and managing patient flow to maximize provider productivity. - Policy Development
Establishing standard operating procedures, clinical protocols, and comprehensive risk management strategies.
Revenue Cycle Management (Week 21)
Telehealth billing codes (E/M, modifier 95, POS 02/10)
Genetics-specific coding (test CPTs, Z-codes)
Prior authorization and medical necessity documentation
Denial management and appeals processes
Financial forecasting and breakeven analysis
Patient Acquisition Strategy (Week 22)
Compliant digital marketing for healthcare services
Building referral networks and provider education
Patient education programs and conversion funnels
Accessibility initiatives and community partnerships
Patient satisfaction measurement and service recovery
Business Performance Metrics
0
30
60
90
New
Patient
Visits
per...
Follow-up
Conversion
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Genetic Test... Days in A/R Patient Satisfaction...
Initial T arget Established Practice
These business modules provide practical tools and templates that participants can immediately implement in their practice planning, from financial pro formas to marketing calendars and operational checklists.
▶ Holistic and Integrative Approaches
Genetic testing provides powerful insights, but optimal patient outcomes often require complementary approaches that address modifiable factors. This module presents evidence-aligned adjunctive strategies that telegenetics providers can incorporate into patient care plans.
- Evidence-based screening tools to identify candidates for complementary interventions
- Telehealth-compatible resources and digital tools for patient self-management
- Virtual referral networks for specialized integrative services
- Documentation templates that appropriately incorporate holistic recommendations
- Clear communication frameworks that distinguish between established medical recommendations and complementary approaches
Lifestyle Medicine
Evidence-based dietary patterns (Mediterranean, DASH), physical activity prescriptions, sleep optimization protocols, tobacco cessation, and alcohol moderation strategies.
Stress Reduction
Mindfulness-based stress reduction techniques, cognitive behavioral therapy approaches, therapeutic yoga, breathing exercises, and CBT-I for insomnia management.
Targeted Nutrition
Condition-specific nutritional interventions with scientific support, such as folate supplementation during pregnancy, vitamin D for documented deficiency, and omega-3 fatty acids for hypertriglyceridemia.
Supportive Therapies
Complementary approaches for symptom management, including acupuncture for chemotherapy-induced nausea, pelvic floor therapy, genetics-informed nutrition counseling, and pain self-management programs.
Social Support
Genetic condition-specific peer groups, social work referrals, financial navigation services, and community resource connections to address social determinants of health.
▶ Popular Telegenetics Services You Can Offer
Service Models and Clinical Applications
Upon completion of the program, graduates will be equipped to establish various specialized telegenetics services designed to meet specific patient needs and market demands. These service models can be implemented as standalone offerings or combined to create a comprehensive telegenetics practice.
Virtual Hereditary Cancer Clinic
Risk assessment, genetic testing, and cascade screening for families with cancer predisposition syndromes. Includes results interpretation, management recommendations, and coordination with oncology providers.
Cardiogenetics eConsult Program
Specialized genetic evaluation for inherited cardiac conditions, with remote cascade screening protocols and integration with cardiology practices for comprehensive management.
Pharmacogenomics Service
Personalized medication management consultations focused on psychiatric medications, cardiovascular drugs, pain management, and cancer therapeutics based on genetic profile.
Reproductive Genetics Program
Preconception carrier screening, prenatal testing navigation, and genetic counseling for prospective and expectant parents, with clear referral pathways for diagnostic procedures.
Pediatric Neurogenetics Service
Specialized evaluation and care coordination for children with suspected genetic neurological conditions, including exome sequencing interpretation and multidisciplinary care planning.
Precision Oncology Consultation
Expert second opinion service for tumor genomic profiling interpretation, targeted therapy recommendations, and clinical trial matching for patients with advanced cancers.
Undiagnosed Disease Program
Comprehensive genomic evaluation service for complex, previously undiagnosed conditions, featuring virtual case review boards and coordinated diagnostic strategies.
Enterprise Genetics Support
B2B services including employer genetic benefit management, primary care genetics consultation lines, and health system integration programs.
▶ Hereditary Cancer and Cardiogenetics Conditions
Hereditary Cancer Syndromes
Hereditary Breast and Ovarian Cancer
BRCA1/2-related cancers and moderate-risk genes including PALB2, CHEK2, and ATM, with risk-appropriate screening and preventive options.
Lynch Syndrome and Polyposis
MLH1, MSH2, MSH6, PMS2, EPCAM mutations (Lynch); APC and MUTYH variants (polyposis) with colorectal and extracolonic cancer risks.
Multi-Cancer Predisposition
Li-Fraumeni (TP53), Cowden (PTEN), Peutz-Jeghers (STK11), and hereditary diffuse gastric cancer (CDH1) syndromes requiring comprehensive surveillance.
Endocrine and Neuroendocrine Tumors
Paraganglioma/pheochromocytoma (SDHx), MEN1/MEN2, VHL, and neurofibromatosis (NF1/NF2) with complex management needs.
Cardiogenetic Conditions
Arrhythmia Syndromes
Long QT syndrome, Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia (CPVT), and other channelopathies affecting cardiac conduction.
Cardiomyopathies
Hypertrophic, dilated, restrictive, and arrhythmogenic cardiomyopathies with varying genetic etiologies and phenotypic expression.
Aortopathies
Marfan syndrome (FBN1), Loeys-Dietz syndrome (TGFBR1/2), vascular Ehlers-Danlos (COL3A1), and familial thoracic aortic aneurysm/dissection.
Lipid Disorders
Familial hypercholesterolemia (LDLR/APOB/PCSK9) and other inherited dyslipidemias affecting cardiovascular risk profiles.
These condition categories represent core areas where telegenetics services can provide significant clinical value through risk assessment, genetic testing, family screening, and management guidance. The program provides detailed modules on each condition group, including testing algorithms, management guidelines, and telehealth-specific implementation considerations.
▶ Neurogenetic, Neuromuscular and Metabolic Conditions
Trinucleotide Repeat Disorders
Huntington disease and Fragile X syndrome, characterized by expanding nucleotide repeats with complex inheritance patterns and neurological manifestations.
Neurodevelopmental Syndromes
Tuberous sclerosis, Rett syndrome, and Angelman/Prader-Willi syndromes affecting brain development with multisystem involvement.
Progressive Neuromuscular Conditions
Charcot-Marie-Tooth, muscular dystrophies, spinal muscular atrophy, and myotonic dystrophy requiring comprehensive management strategies.
Neurodegeneration and Movement
Hereditary ataxias, Wilson disease, and genetic forms of ALS with variable age of onset and progression trajectories.
Epilepsy Genetics
Single-gene epilepsy syndromes involving sodium and potassium channels (SCN1A/2A, KCNQ2) and other pathways affecting neuronal excitability.
Tumor Predisposition Syndromes
Neurofibromatosis 1/2 and schwannomatosis with CNS and peripheral nervous system tumor risks requiring surveillance.
Amino Acid Disorders
Phenylketonuria, maple syrup urine disease, and homocystinuria affecting protein metabolism with potential for severe neurological complications if untreated.
Urea Cycle Defects
OTC, ASS1, and ASL deficiencies disrupting ammonia detoxification with risk for hyperammonemia and encephalopathy requiring careful management.
Fatty Acid Oxidation Disorders
MCAD, VLCAD, and LCHAD deficiencies affecting energy metabolism with risk for hypoglycemia, cardiomyopathy, and other complications during metabolic stress.
Mitochondrial Disorders
POLG-related conditions and mitochondrial DNA variants causing energy production defects with multisystem involvement and heterogeneous presentation.
Lysosomal Storage Diseases
Gaucher, T ay-Sachs, Niemann-Pick, and Krabbe disease characterized by enzyme deficiencies leading to substrate accumulation and progressive cellular dysfunction.
Telegenetics services for these complex conditions focus on test selection, results interpretation, and coordination with local specialists for ongoing management. The program provides detailed protocols for multidisciplinary collaboration in these cases.
▶ Hematology, Immunology, Endocrine and Connective Tissue Disorders
Hematology and Immunology
Hemochromatosis (HFE): Iron overload disorder with simple genetic testing but complex penetrance considerations
Hemoglobinopathies: Alpha/beta-thalassemia and sickle cell disease requiring comprehensive counseling about reproductive risks and clinical management
G6PD Deficiency: X-linked enzyme deficiency with medication and dietary triggers requiring personalized avoidance guidance
Primary Immunodeficiencies: Severe combined immunodeficiency (SCID), common variable immunodeficiency (CVID), and chronic granulomatous disease (CGD) with complex management needs
Hereditary Angioedema: SERPING1 mutations affecting complement regulation with implications for emergency treatment protocols
Thrombophilias: Factor V Leiden and prothrombin gene variants with nuanced risk assessment and management considerations
Endocrine and Renal Disorders
Monogenic Diabetes: MODY subtypes and neonatal diabetes with implications for treatment selection and family screening
Adrenal Disorders: Congenital adrenal hyperplasia and disorders of sex development requiring sensitive counseling approaches
Multiple Endocrine Neoplasia: MEN1 and MEN2 syndromes with complex surveillance requirements across multiple organ systems
Polycystic Kidney Disease: PKD1/2-related autosomal dominant polycystic kidney disease requiring long-term monitoring
Inherited Nephropathies: Alport syndrome and salt-wasting disorders (Bartter/Gitelman) with implications for renal management
Dermatologic and Connective Tissue Disorders
Ehlers-Danlos Spectrum
Varied subtypes affecting collagen and connective tissue, ranging from hypermobility to life-threatening vascular complications, requiring multidisciplinary management.
Osteogenesis Imperfecta
Brittle bone disease with varying severity based on specific collagen mutations, requiring coordinated care with orthopedics, physical therapy, and pain management.
Genodermatoses
Xeroderma pigmentosum with extreme UV sensitivity and cancer risk; epidermolysis bullosa affecting skin integrity with varying severity and management approaches.
Hemochromatosis-Related Manifestations
Counseling regarding skin findings associated with hereditary hemochromatosis, including bronze discoloration, and their relationship to iron overload status.
These diverse conditions present unique telegenetic counseling challenges and opportunities. The program provides specialized modules on developing cultural competency, addressing health literacy barriers, and creating accessible telehealth services for patients with these genetic conditions.
▶ Ophthalmologic, Otolaryngology, and Reproductive Genetics
Ophthalmologic Conditions
Retinitis Pigmentosa: Progressive retinal degeneration with genetic heterogeneity
Stargardt Disease: Macular degeneration with childhood or early adult onset
Leber Congenital Amaurosis: Severe visual impairment from birth
Usher Syndrome: Combined hearing and vision loss with variable onset
Otolaryngology Genetics
GJB2/6-Related Hearing Loss: Common cause of congenital deafness
Waardenburg Syndrome: Hearing loss with pigmentary abnormalities
Usher Syndrome: Progressive hearing and vision loss
Syndromic Hearing Loss: Multiple gene panels for complex presentations
Reproductive Genetics
Carrier Screening: Cystic fibrosis, SMA, Fragile X premutation
Hemoglobinopathy Screening: Sickle cell, thalassemias
NIPS Counseling: Interpretation of non-invasive prenatal screening
Recurrent Pregnancy Loss: Genetic factors including translocations
▶ Pharmacogenomic Applications
Pharmacogenomics (PGx) identifies genetic variations that influence medication response, allowing for personalized prescribing that can improve efficacy and reduce adverse effects. Key actionable gene-drug pairs covered in the program include:
- CYP2D6
Impacts metabolism of many medications including codeine, tramadol, and certain antidepressants. Poor metabolizers may experience reduced efficacy with codeine while ultrarapid metabolizers face increased toxicity risk. - CYP2C19
Affects activation of clopidogrel (blood thinner) and metabolism of many SSRIs. Poor metabolizers may have reduced clopidogrel efficacy with increased cardiovascular event risk. - SLCO1B1
Variant carriers have increased risk of simvastatin-induced myopathy (muscle damage), requiring dose adjustment or alternative statin selection. - HLA Alleles
HLA-B*57:01 carriers risk severe hypersensitivity to abacavir (HIV medication); HLA-B*15:02 carriers have increased risk of severe skin reactions with carbamazepine. - TPMT/NUDT15
Affect metabolism of thiopurine drugs used in autoimmune conditions and cancer treatment, with variant carriers requiring significant dose reductions.
The program provides detailed protocols for implementing PGx testing services, including clinical decision support integration, result interpretation guidelines, and payer coverage navigation.
▶ Compliance Curriculum Details
HIPAA Privacy Rule Implementation
Practical application of Privacy Rule provisions in telehealth, including patient rights, minimum necessary standards, authorized disclosures, Notice of Privacy Practices, and special protections for genetic information.
Security Rule Safeguards
Comprehensive implementation of administrative safeguards (risk analysis, security officer, training), physical safeguards (workstation security, device controls), and technical safeguards (access controls, audit logs, encryption, transmission security) for telegenetics.
Business Associate Management
Creating and managing compliant Business Associate Agreements (BAAs) with telehealth platforms, cloud storage providers, billing services, and other vendors handling protected health information.
Breach Response Protocols
Developing breach detection systems, incident response procedures, documentation requirements, notification timelines, and mitigation strategies aligned with HITECH requirements.
ONC Cures Act Requirements
Information blocking prohibition and exceptions
Patient electronic health information access
API implementation for data exchange
USCDI data element compliance
FHIR-based interoperability standards
OSHA Compliance for Telehealth
Remote workstation ergonomics standards
Bloodborne pathogen protocols for kit handling
Hazard communication requirements
Emergency action planning for remote teams
Documentation and training requirements
- Written Policies and Procedures
Developing comprehensive documentation covering all aspects of telegenetics practice, including code of conduct, billing policies, and genetic testing protocols. - Compliance Officer and Committee
Establishing compliance leadership structure with appropriate authority, reporting mechanisms, and dedicated resources. - Effective Training and Education
Implementing initial and ongoing compliance education for all staff, with specialized modules for telehealth, genetic testing, and billing functions. - Communication Channels
Creating accessible reporting systems for compliance concerns, including anonymous options and non-retaliation protections. - Monitoring and Auditing
Developing systematic review processes for high-risk areas including telehealth documentation, genetic test ordering, and claim submission. - Consistent Enforcement
Establishing disciplinary standards and incentives to promote compliance culture throughout the organization. - Prompt Response to Issues
Creating investigation protocols, corrective action procedures, and self-disclosure policies for identified compliance problems.
The program provides comprehensive compliance templates, risk assessment tools, and audit checklists that participants can customize for their specific telegenetics practice model.
▶ Enrollment Process and Program Fees
The TeleMedical Genetics professional program requires a total investment of $1,969, structured to cover all aspects of your comprehensive training experience.
Covers application processing, eligibility verification, and personalized track selection to ensure optimal program fit.
Provides access to HIPAA-compliant video conferencing, secure messaging, and practice management platforms for hands-on learning.
Covers core instructional content and specialized modules delivered by industry experts throughout the 24-week program.
Includes all evaluations and assessments, plus formal credentialing documentation upon successful program completion.
Provides comprehensive digital and physical resources, clinical guidelines, and specialty protocols for practice implementation.
Supports job placement assistance, patient acquisition strategies, and business development coaching following program completion.
- Flexible Payment Plans
Option 1: Full payment of $1,969 at enrollment
Option 2: Split payment with $899 due at enrollment and the remaining balance due at course completion - Contact Information
Website: www.T elehealth.school
Email: info@telehealth.school
Phone: (848) 233-3332 - Quarterly Cohort Schedule
Cohort Application Program Dates
Spring By Feb 15 Mar 1 3 Aug 31
Summer By May 15 Jun 1 3 Nov 30
Fall By Aug 15 Sep 1 3 Feb 28
Winter By Nov 15 Dec 1 3 May 31 - Enrollment Process
Complete online application at www.T elehealth.school/apply
1.
Schedule consultation call with admissions team 2.
Submit documentation and select payment option 3.
Gain immediate access to orientation materials 4.
▶ Day-in-the-Life: Running a Telegenetics Clinic
This sample schedule illustrates the typical flow of a fully operational telegenetics practice, demonstrating how providers balance direct patient care with administrative responsibilities and professional development.
- 7:45 - 8:00 AM: Morning Setup
Complete security check and system login. Review overnight messages, lab alerts, and daily dashboard metrics to prepare for patient encounters. - 8:00 - 8:10 AM: Daily Huddle
Conduct brief team meeting to review caseload, identify potential escalations, and confirm coverage arrangements for the day. - 8:10 - 8:30 AM: Pre-visit Preparation
Review scheduled patients' pedigrees, clinical indications, and insurance prerequisites to ensure efficient consultations. - 8:30 AM - 12:00 PM: New Consultations
Conduct six 30-35 minute initial telegenetics consultations across different service lines (hereditary cancer, pharmacogenomics, prenatal). Complete electronic consent, test selection, and home kit ordering during sessions. - 12:00 - 12:30 PM: Administrative Break
Quick lunch while managing message inbox and submitting prior authorization requests for ordered genetic tests. - 12:30 - 2:30 PM: Results Consultations
Deliver test results to three patients in 30-40 minute sessions. Provide summary letters, management templates, and cascade testing information for family members. - 2:30 - 3:00 PM: Multidisciplinary Conference
Participate in virtual case review board with specialists from oncology, cardiology, and genomics to discuss complex cases. - 3:00 - 4:00 PM: Documentation and Billing
Complete clinical documentation, finalize billing codes, verify modifiers, and review claims for submission. - 4:00 - 4:45 PM: Practice Development
Conduct outreach activities including referral liaison calls and educational webinar preparation to build practice visibility. - 4:45 - 5:30 PM: Professional Development
Dedicate time to learning activities including variant curation, journal review, and standard operating procedure updates.
The program provides detailed workflow templates, scheduling optimization tools, and efficiency strategies to help participants maximize productivity while maintaining quality care and work-life balance in telegenetics practice.
▶ Teaching Case Studies
The program incorporates realistic case studies that illustrate common challenges in telegenetics practice. Each case focuses on specific learning objectives related to both clinical management and telehealth implementation.
BRCA1 VUS Management
Patient: 42-year-old with triple-negative breast cancer; panel testing returns variant of uncertain significance.
Learning Objectives: Applying evidence-based management without VUS-driven surgical decisions; developing cascade testing strategies; implementing variant reclassification monitoring; creating insurer-friendly documentation.
Lynch Syndrome Case
Patient: 37-year-old with MMR-deficient colon tumor; germline PMS2 pathogenic variant identified.
Learning Objectives: Creating effective family communication letters; developing appropriate screening protocols; implementing interstate cascade testing workflows; mastering complex billing scenarios for genetic counseling and testing.
Hypertrophic Cardiomyopathy
Patient: 22-year-old athlete with abnormal echocardiogram; MYBPC3 variant identified.
Learning Objectives: Constructing family screening algorithms; developing remote phenotype monitoring plans; creating counseling scripts for athletic participation guidance.
Familial Hypercholesterolemia
Patient: 45-year-old with LDL 230 mg/dL; LDLR variant identified with concurrent PGx testing for SLCO1B1.
Learning Objectives: Implementing cascade screening kit distribution; navigating insurance prior authorization; providing integrated risk management.
Psychiatric Pharmacogenomics
Patient: 34-year-old with multiple SSRI failures; identified as CYP2C19 ultrarapid metabolizer.
Learning Objectives: Configuring clinical decision support alerts; coordinating medication changes with prescribers; tracking outcomes for quality improvement.
Positive NIPS for Trisomy 21
Patient: 31-year-old at 12 weeks gestation with positive non-invasive prenatal screening.
Learning Objectives: Providing balanced counseling on screening vs diagnostic testing; coordinating invasive procedures; delivering non-directive support; documenting time-based billing.
Additional cases cover pediatric neurodevelopmental delay, hereditary paraganglioma, adult-onset mitochondrial disease, and precision oncology scenarios. Each case includes complete documentation templates, billing examples, and telehealth implementation guidance that participants can adapt for their practice.
▶ Financial Potential Model
This illustrative model provides a realistic perspective on the potential financial outcomes of a telegenetics practice. Actual results will vary based on numerous factors including geographic location, payer mix, and practice efficiency.
$0.00
$600,000.00
$1,200,000.00
$1,800,000.00
Weekly (46.2 visits) Monthly (200 visits) Quarterly (600 visits) Annual (2400 visits)
Minimum ($95/visit) Maximum ($700/visit)
Revenue Drivers
Visit Volume: T arget of 200 completed encounters monthly
Service Mix: Range from simple follow-ups ($95) to comprehensive new evaluations ($700)
Payer Contracts: Negotiated rates with insurers significantly impact revenue
Geographic Reach: Multi-state licensure expands potential patient base
Test Selection: Appropriate ordering patterns maximize clinical value and reimbursement
Expense Considerations
35-45% Staffing
Provider compensation, administrative support, genetic counseling assistants
10-15% T echnology
Telehealth platform, EHR, laboratory interfaces, secure communications
5-10% Operations
Licensing, malpractice insurance, test kits, billing services
The program provides detailed financial planning tools, including pro forma templates, breakeven calculators, and payer mix optimization strategies to help participants develop realistic business projections for their specific telegenetics practice model.
▶ Career Pathway and Key References
Upon program completion, graduates are equipped with practical deliverables ready for immediate implementation:
- Practice Blueprint
Comprehensive business plan including service definition, market analysis, operational framework, and financial projections tailored to your specific telegenetics focus. - Compliance Documentation
Complete set of policies, procedures, forms, and risk assessment tools meeting HIPAA, HITECH, OIG, and other regulatory requirements for telegenetics practice. - Marketing Plan
Strategic marketing framework including target audience definition, messaging development, channel selection, and campaign calendar for practice growth. - Practice Implementation Tools
Mock audit protocols, payer enrollment workbooks, contracting templates, and vendor evaluation matrices to streamline practice launch.
The program includes job search coaching, portfolio review, and employer introductions through the placement assistance component. While employment is not guaranteed, these resources enhance your marketability and help you effectively showcase your specialized skills.
Practice Ownership TrackFor those pursuing independent practice, the program provides entity formation guides, contract templates, payer enrollment checklists, and vetted vendor referrals to facilitate practice establishment.
Industry Standards and GuidelinesThe program curriculum aligns with authoritative resources including:
ACMG/AMP variant classification standards
NSGC practice guidelines and telehealth statements
NCCN Genetic/Familial Risk Assessment guidelines
AHA/ACC/HRS cardiac genetics statements
ACOG/SMFM prenatal genetics bulletins
CPIC pharmacogenomics guidelines
Clinical Resources
ClinVar, gnomAD, OMIM, and HGMD databases for variant interpretation; CPIC guidelines for pharmacogenomics ( cpicpgx.org); MotherToBaby teratogen information services
Regulatory Guidance
HHS/OCR HIPAA resources ( hhs.gov/hipaa); ONC Cures Act materials (healthit.gov); OIG Compliance Program Guidance ( oig.hhs.gov); OSHA standards (osha.gov)
Quality Standards
CLIA regulations and CAP accreditation checklists; FDA frameworks for diagnostic testing; ISO/IEC 27001 security management; SAMHSA/42 CFR Part 2 sensitive data guidelines
The program provides a comprehensive digital library with organized access to these resources, enabling graduates to maintain current knowledge and practice standards after program completion.
▶ What You Build During the Course
Throughout the 24-week program, participants progressively develop the complete toolkit needed to launch and operate a successful telegenetics practice. These deliverables provide immediate value upon program completion.
Complete SOP Library
Comprehensive set of standard operating procedures covering privacy, security, testing protocols, genetic counseling workflows, and billing processes, all customized for telehealth delivery.
Security Framework
Detailed security risk analysis template, vulnerability assessment tools, and mitigation planning matrix aligned with HIPAA Security Rule requirements for telegenetics practice.
Health IT Integration Map
Technical architecture diagram with EHR, telehealth platform, and laboratory system connections, including FHIR endpoint specifications and data flow documentation.
Financial Toolkit
Comprehensive pricing structure, payer contracting templates, revenue cycle workflows, and financial projection models tailored to telegenetics services.
Patient Journey Assets
Complete set of patient-facing materials including electronic consent forms, pre-visit questionnaires, pedigree collection tools, results letters, and cascade testing protocols.
Quality Management System
Interactive dashboard for tracking key performance indicators including access metrics, turnaround times, patient satisfaction scores, and revenue cycle performance.
The program culminates in a comprehensive capstone project that synthesizes all course elements into a cohesive, executable plan for launching your TeleMedical Genetics practice. This detailed blueprint includes implementation timelines, resource requirements, staffing models, technology specifications, and marketing strategies tailored to your specific practice vision.
With these deliverables in hand, graduates are positioned to efficiently implement their telegenetics service, whether as an independent practice, a service line within an existing organization, or a specialized consulting offering.