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FamGenix

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uuid003vo5j

Namestring
FamGenix
Legal namestring
FamHis, Inc.
Websiteurl
famgenix.com
Company typeenum
Private
Founded yearint
2019
Descriptiontext

FamGenix, Inc. (legal entity FamHis, Inc., dba FamGenix; headquartered in Fargo, ND with prior offices in Boynton Beach and Delray Beach, FL) builds a cloud-based family health history and pedigree platform that helps clinicians and patients assess hereditary disease risk. The platform is deployed on AWS with regional data residency in the US, Canada, the EU/UK, and Australia/Asia-Pacific, and is HIPAA- and GDPR-compliant (SOC 2 Type 1 completed April 2026, Type 2 in progress). Core products include the Provider Portal (a pedigree chart maker with built-in medical ontology — HPO, OMIM, CHV, NCI, HGNC — and automated guideline-based identification of patients meeting NCCN/ACMG/ASBrS referral criteria), the Patient App (a free mobile/web family health history questionnaire in English, Spanish, French, German, and Dutch with the FamShare family data-sharing feature), the Clinicians Platform (enterprise tier with EHR integration and API), a White Label/Embedded integration offer, and a Risk Server API that sub-licenses validated cancer and cardiovascular risk models (BOADICEA v6, Tyrer-Cuzick v8, BayesMendel, Gail, Claus, QRISK3). The company sells through a hybrid GTM: direct enterprise field sales to healthcare systems and clinical genetics teams, OEM/embedded and white-label licensing to EHR and clinical platforms, and a freemium direct-to-consumer channel via the free patient app on iOS and Android. Revenue is generated through individual subscriptions ($500/year per license), tiered enterprise contracts, and add-on fees for advanced risk models, custom questionnaires, EHR integration, and API access. Distribution is supported by partnerships with My Gene Counsel (March 2025) and Spesana (December 2023), and customer logos include City of Hope, UCSF, Boston Children's, Sharp HealthCare, Allina Health, UnityPoint Health, MercyOne, NHS Liverpool, and Cork University Hospital.

Short descriptiontext

FamGenix is a cloud-based family health history and pedigree platform that helps clinicians, genetic counselors, and patients assess hereditary disease risk, serving healthcare providers, EHR partners, and individual patients across the US, Canada, the EU/UK, and Australia.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersBoynton Beach, United States
HQ citystring
Boynton Beach
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices7 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
pedigree drawing software, genetic risk assessment, family health history, clinical genetics tools, hereditary cancer screening
NAICS code2 codes
  • Computer Systems Design and Related Services54151
  • Computer Systems Design Services541512
SIC code1 code
  • Services-Computer Integrated Systems Design7373
Product category
Clinical Genetics Software
Social media profiles2 records
GTM motion3 records

Each record includes

Type, Description, Source

Revenue model7 records
1Individual Subscription License
TypeSubscription Recurring
Description

Annual subscription license at $500/year for single-user access with unlimited pedigrees. Includes basic features with additional fees for premium add-ons like advanced risk models and patient questionnaires.

famgenix.com
2Premium Enterprise License
TypeSubscription Recurring
Description

Tiered pricing model for multi-user enterprise deployments with full feature access including multi-user access, EHR integration, API access, and custom branding. Additional fees apply for custom features.

famgenix.com
3Risk Model Licensing (Add-on)
TypeLicensing Royalties
Description

Additional fee add-ons for individual risk assessment models: BOADICEA (+$100), Tyrer-Cuzick v8 (+$100), BayesMendel (+$100). Gail and Claus models included in base Individual license.

famgenix.com
4Patient Questionnaire Add-on
TypeSubscription Recurring
Description

Additional fee for standard or custom patient questionnaires and surveys. Standard questionnaires available as additional fee on Individual tier; custom data fields, questionnaires and surveys available as additional fee on both tiers.

famgenix.com
5White-Label/Embedded Integration Licensing
TypeLicensing Royalties
Description

Embedding FamGenix pedigree and risk assessment functionality into existing clinical systems with flexible licensing based on specific needs. Includes SSO integration and maintains patient data control within existing systems.

famgenix.com
6API Risk Model Sub-licensing
TypeLicensing Royalties
Description

Send family history data to FamGenix risk server via API to calculate and return results for display in customer's existing system. Enables risk model usage without full platform deployment.

famgenix.com
7Free Patient App
TypeFreemium
Description

Free mobile and web app for patients to record and maintain family health history, assess hereditary disease risk, and share with family members. Revenue generated from healthcare provider licensing of the platform that connects to patient data.

famgenix.com
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels4 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components6 values
Personnel, Technology or R&D, Infrastructure, Marketing or Sales, Operations, Others
Pricing details2 tiers
1Individual license for single users at $500/yr with unlimited pedigrees
ModelSubscriptionBilling cadenceAnnual
Notes

$500/year per license. Includes: unlimited pedigree drawing, built-in medical ontology for disease/gene tracking, genetic testing results tracking, NCCN and ACMG/NSGC guidelines, query/filter patient data, Gail and Claus cancer risk models, hosted in USA, CAN, EU/UK, or Australia/Asia Pacific. Additional fees: Tyrer-Cuzick v8, BOADICEA, BayesMendel, QRISK each +$100; standard patient questionnaires +$500; custom surveys/questionnaires at additional fee.

famgenix.com
2Premium enterprise tier with tiered pricing for multi-user access and full integration capabilities
ModelSubscriptionBilling cadenceAnnual
Notes

Tiered pricing (not publicly disclosed). Includes all Individual features plus: multi-user access to all pedigrees and data, EHR integration (view-only or editable), API access for data exchange, custom branding with own logos and colors. All add-ons (custom surveys, advanced risk models) available as additional fees.

famgenix.com
GTM typeB2B
B2B
Offering typeSoftware
Software
Core offering1 text field

FamGenix provides a cloud-based family health history platform combining a pedigree drawing tool, integrated cancer and cardiovascular genetic risk assessment models, and a patient-facing mobile/web app. The platform enables clinicians, genetic counselors, and health systems to capture family health history, generate pedigrees, run multiple risk models simultaneously, and automatically identify patients meeting NCCN/ACMG referral criteria. It is offered through Individual subscriptions, Premium enterprise licenses, white-label/embedded OEM integrations, and a Risk Server API for existing clinical systems.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • Patients meeting referral criteria are automatically identified based on NCCN/ACMG/ASBrS guidelines, displaying specific reasons criteria was met
+3 more records
Product overview1 text field

FamGenix offers a unified family health history platform with three core components: the Provider Portal (a comprehensive pedigree drawing and genetic risk assessment tool for clinicians), the Patient App (a mobile/web application for family health history collection available in English, Spanish, French, German, and Dutch), and the Clinicians Platform (an enterprise solution combining all tools with EHR integration and API access). The platform integrates multiple cancer and cardiovascular risk assessment models (BOADICEA, Tyrer-Cuzick, BayesMendel, Gail, Claus, QRISK3) that run simultaneously to calculate 5-year, 10-year, and lifetime hereditary disease risk. The system automatically identifies patients meeting NCCN/ACMG clinical guidelines for genetic counseling referral. White-label and API options enable integration into existing clinical systems and custom branded deployments.

Scale indicator5 records

Each record includes

Type, Value, Description, Source

Partnership3 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-03-18
Description

Strategic partnership announced March 18, 2025 to provide healthcare centers with comprehensive digital genetic risk assessment and education toolkit. Combined platform facilitates risk assessment for hereditary cancer, cardiovascular disease, kidney disease, lymphoma, reproductive disorders, rare diseases, and other genetic conditions. Includes pre-test and post-test genetic education and ongoing dynamic updates specific to genetic test results.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2023-12-18
Description

Strategic partnership announced December 18, 2023 to advance precision medicine and integrate FamGenix hereditary risk screening with Spesana's clinical workflow ecosystem. FamGenix pedigree and hereditary risk assessment solutions planned to be seamlessly integrated with Spesana's solution, providing comprehensive tools for clinicians at point of care. Both companies committed to making family health histories part of every patient's electronic health record.

Strategic tierCoreTypeTechnology or IntegrationAnnounced on2020-01-01
Description

Cloud infrastructure provider using AWS with dedicated regional servers in US, Canada, EU, UK, and Australia. AWS core infrastructure designed to meet most stringent security requirements for healthcare, banks, and military. Enables FamGenix to achieve and monitor HIPAA and GDPR compliance. Most extensive global network of regions ensures consistent security and compliance standards across all deployments.

Recent move9 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat6 records

Each record includes

Type, Details

Customer concentration

Classification, Details

Named customers16 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile3 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

API detail
Has APIbool
Yes

Docs URL, Description

AI capability3 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature7 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
No data
Compliance3 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds4 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

FamGenix

Clinical Genetics Softwarefamgenix.com

FamGenix is a cloud-based family health history and pedigree platform that helps clinicians, genetic counselors, and patients assess hereditary disease risk, serving healthcare providers, EHR partners, and individual patients across the US, Canada, the EU/UK, and Australia.

What FamGenix does

FamGenix, Inc. (legal entity FamHis, Inc., dba FamGenix; headquartered in Fargo, ND with prior offices in Boynton Beach and Delray Beach, FL) builds a cloud-based family health history and pedigree platform that helps clinicians and patients assess hereditary disease risk. The platform is deployed on AWS with regional data residency in the US, Canada, the EU/UK, and Australia/Asia-Pacific, and is HIPAA- and GDPR-compliant (SOC 2 Type 1 completed April 2026, Type 2 in progress). Core products include the Provider Portal (a pedigree chart maker with built-in medical ontology — HPO, OMIM, CHV, NCI, HGNC — and automated guideline-based identification of patients meeting NCCN/ACMG/ASBrS referral criteria), the Patient App (a free mobile/web family health history questionnaire in English, Spanish, French, German, and Dutch with the FamShare family data-sharing feature), the Clinicians Platform (enterprise tier with EHR integration and API), a White Label/Embedded integration offer, and a Risk Server API that sub-licenses validated cancer and cardiovascular risk models (BOADICEA v6, Tyrer-Cuzick v8, BayesMendel, Gail, Claus, QRISK3). The company sells through a hybrid GTM: direct enterprise field sales to healthcare systems and clinical genetics teams, OEM/embedded and white-label licensing to EHR and clinical platforms, and a freemium direct-to-consumer channel via the free patient app on iOS and Android. Revenue is generated through individual subscriptions ($500/year per license), tiered enterprise contracts, and add-on fees for advanced risk models, custom questionnaires, EHR integration, and API access. Distribution is supported by partnerships with My Gene Counsel (March 2025) and Spesana (December 2023), and customer logos include City of Hope, UCSF, Boston Children's, Sharp HealthCare, Allina Health, UnityPoint Health, MercyOne, NHS Liverpool, and Cork University Hospital.

FamGenix firmographics

Firmographics
Name
FamGenix
Legal name
FamHis, Inc.
Website
https://famgenix.com
Company type
Private
Founded year
2019
Operating status
Operating
Headcount range
1–10 employees
Short description
FamGenix is a cloud-based family health history and pedigree platform that helps clinicians, genetic counselors, and patients assess hereditary disease risk, serving healthcare providers, EHR partners, and individual patients across the US, Canada, the EU/UK, and Australia.
Ownership category
akta.pro rank

Where FamGenix is headquartered

Location

Headquarters

HQ city
Boynton Beach
HQ country
United States
HQ region
North America

Offices7 records

Markets served

FamGenix business model

Business model
GTM type
B2B
Offering type
Software
Cost components
Personnel, Technology or R&D, Infrastructure, Marketing or Sales, Operations, Others

Revenue model

  1. Individual Subscription License: Annual subscription license at $500/year for single-user access with unlimited pedigrees. Includes basic features with additional fees for premium add-ons like advanced risk models and patient questionnaires.
  2. Premium Enterprise License: Tiered pricing model for multi-user enterprise deployments with full feature access including multi-user access, EHR integration, API access, and custom branding. Additional fees apply for custom features.
  3. Risk Model Licensing (Add-on): Additional fee add-ons for individual risk assessment models: BOADICEA (+$100), Tyrer-Cuzick v8 (+$100), BayesMendel (+$100). Gail and Claus models included in base Individual license.
  4. Patient Questionnaire Add-on: Additional fee for standard or custom patient questionnaires and surveys. Standard questionnaires available as additional fee on Individual tier; custom data fields, questionnaires and surveys available as additional fee on both tiers.
  5. White-Label/Embedded Integration Licensing: Embedding FamGenix pedigree and risk assessment functionality into existing clinical systems with flexible licensing based on specific needs. Includes SSO integration and maintains patient data control within existing systems.
  6. API Risk Model Sub-licensing: Send family history data to FamGenix risk server via API to calculate and return results for display in customer's existing system. Enables risk model usage without full platform deployment.
  7. Free Patient App: Free mobile and web app for patients to record and maintain family health history, assess hereditary disease risk, and share with family members. Revenue generated from healthcare provider licensing of the platform that connects to patient data.

Pricing tiers

ModelBillingPrice
SubscriptionAnnualIndividual license for single users at $500/yr with unlimited pedigrees
SubscriptionAnnualPremium enterprise tier with tiered pricing for multi-user access and full integration capabilities

Go-to-market motion3 records

Distribution channels4 records

Marketing channels6 records

FamGenix product offering

Product offering

Core offering

FamGenix provides a cloud-based family health history platform combining a pedigree drawing tool, integrated cancer and cardiovascular genetic risk assessment models, and a patient-facing mobile/web app. The platform enables clinicians, genetic counselors, and health systems to capture family health history, generate pedigrees, run multiple risk models simultaneously, and automatically identify patients meeting NCCN/ACMG referral criteria. It is offered through Individual subscriptions, Premium enterprise licenses, white-label/embedded OEM integrations, and a Risk Server API for existing clinical systems.

Product overview

FamGenix offers a unified family health history platform with three core components: the Provider Portal (a comprehensive pedigree drawing and genetic risk assessment tool for clinicians), the Patient App (a mobile/web application for family health history collection available in English, Spanish, French, German, and Dutch), and the Clinicians Platform (an enterprise solution combining all tools with EHR integration and API access). The platform integrates multiple cancer and cardiovascular risk assessment models (BOADICEA, Tyrer-Cuzick, BayesMendel, Gail, Claus, QRISK3) that run simultaneously to calculate 5-year, 10-year, and lifetime hereditary disease risk. The system automatically identifies patients meeting NCCN/ACMG clinical guidelines for genetic counseling referral. White-label and API options enable integration into existing clinical systems and custom branded deployments.

Differentiator

Problem solved

Functional benefit

Quantifiable outcome

  • Patients meeting referral criteria are automatically identified based on NCCN/ACMG/ASBrS guidelines, displaying specific reasons criteria was met
  • +3 more outcomes

Companies that use FamGenix

Customer profile

Named customers16 records

Segments3 records

Ideal customer profiles3 records

FamGenix technology and API

Technology

API detail

Has API
Yes
API docs
API detail

Core technology

AI maturity

App detail

AI capability3 records

Feature7 records

FamGenix partnerships and signals

Strategic signal

Partnerships

Three partnerships are on record, tiered core.

  • My Gene CounselcoreStrategic or Co-development Partner · 18 March 2025Strategic partnership announced March 18, 2025 to provide healthcare centers with comprehensive digital genetic risk assessment and education toolkit. Combined platform facilitates risk assessment for hereditary cancer, cardiovascular disease, kidney disease, lymphoma, reproductive disorders, rare diseases, and other genetic conditions. Includes pre-test and post-test genetic education and ongoing dynamic updates specific to genetic test results.
  • SpesanacoreStrategic or Co-development Partner · 18 December 2023Strategic partnership announced December 18, 2023 to advance precision medicine and integrate FamGenix hereditary risk screening with Spesana's clinical workflow ecosystem. FamGenix pedigree and hereditary risk assessment solutions planned to be seamlessly integrated with Spesana's solution, providing comprehensive tools for clinicians at point of care. Both companies committed to making family health histories part of every patient's electronic health record.
  • Amazon Web Services (AWS)coreTechnology or Integration · 1 January 2020Cloud infrastructure provider using AWS with dedicated regional servers in US, Canada, EU, UK, and Australia. AWS core infrastructure designed to meet most stringent security requirements for healthcare, banks, and military. Enables FamGenix to achieve and monitor HIPAA and GDPR compliance. Most extensive global network of regions ensures consistent security and compliance standards across all deployments.

Scale indicators5 records

Recent moves9 records

Expansion highlights6 records

FamGenix competitors and assessment

Company assessment

Market position

Strengths5 records

Weaknesses5 records

Competitive moat6 records

Customer concentration

FamGenix social profiles

Digital presence

FamGenix compliance and trust

Trust signal

Compliance3 records

FamGenix financial estimates

Financial estimate

Revenue estimate

Valuation estimate

FamGenix leadership team

Management profile

Number of profiles

FamGenix funding detail

Funding detail

Funding overview

Funding rounds4 records

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

FamGenix M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about FamGenix

What does FamGenix do?

FamGenix provides a cloud-based family health history platform combining a pedigree drawing tool, integrated cancer and cardiovascular genetic risk assessment models, and a patient-facing mobile/web app. The platform enables clinicians, genetic counselors, and health systems to capture family health history, generate pedigrees, run multiple risk models simultaneously, and automatically identify patients meeting NCCN/ACMG referral criteria. It is offered through Individual subscriptions, Premium enterprise licenses, white-label/embedded OEM integrations, and a Risk Server API for existing clinical systems.

Is FamGenix a public or private company?

FamGenix is a private company. It is classified as founder individual operated bootstrapped and is currently operating.

When was FamGenix founded?

FamGenix was founded in 2019. It employs 1 to 10 people.

Where is FamGenix based?

FamGenix is headquartered in Boynton Beach, United States, in the North America region.

How does FamGenix make money?

Seven revenue lines are on record. Individual Subscription License is the primary driver. The others are premium Enterprise License, risk Model Licensing (Add-on), patient Questionnaire Add-on, white-Label/Embedded Integration Licensing, API Risk Model Sub-licensing and free Patient App.

Does FamGenix have an API?

Yes. FamGenix offers API access for exchanging data to and from existing clinical systems. The Risk Server API allows external systems to pass patient family health history data and receive back genetic risk calculation results for display in their own system. API access is included with Premium/Premium tier licensing; Individual tier offers API access for an additional fee.

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Live signals
MygenecounselMy Gene Counsel and FamGenix Announce Strategic Partnership to Transform Genetic Risk Assessment and Patient EducationMy Gene Counsel and FamGenix announced a strategic partnership to provide healthcare centers with an integrated digital toolkit for genetic risk assessment and patient education. The combined platform enables providers to assess hereditary conditions, deliver tailored pre- and post-test education, and offer ongoing genetic insights to support precision medicine at scale.SecSEC FORM DFamHis, Inc., a Florida-based corporation, filed a Form D with the Securities and Exchange Commission to announce an exempt securities offering under Rule 506(b). The company intends to raise up to $1,000,000 USD, having already sold $300,000 worth of equity securities to one investor as of June 2023. The filing indicates a minimum investment threshold of $100,000 for outside participants.SecSEC FORM DFamHis, Inc. filed a Form D with the SEC for an exempt securities offering under Rule 506(b), claiming a total offering amount of $422,000 USD. The filing indicates that $362,000 has been sold to three investors, with $60,000 remaining to be sold as of December 20, 2022. Michael Brammer, the CEO, signed the notice on behalf of the Florida-based corporation.PR NewswireFamHis, Inc. Completes Its Launch of the FamGenix Family Health History PlatformFamHis, Inc. has completed and launched worldwide its FamGenix family health history platform, which includes a free patient mobile app and a provider portal for clinicians. The platform enables patients to collect, control, and securely share family health history data with healthcare providers and family members through features like FamShare. The company has signed its first white-label license with a cancer center and has servers deployed in the US and Europe, with expansion planned for Canada and Australia.