# gene42.com > AI-optimized mirror of gene42.com containing 24 pages totalling 34,919 words of clean markdown content, structured data, and semantic HTML. Original source: https://gene42.com/. Last updated: 2026-06-15T19:19:24.195Z. Each page is available as HTML (with JSON-LD structured data) and Markdown (text-only, ideal for LLMs and RAG). ## Homepage - [The complete Genomic Health Record](/content/site-root.html): More than just a pedigree maker, PhenoTips is a complete software solution for medical genomics, making your genomics department future-forward and paper-free. (1,964 words) ## Articles & Blog Posts - [Pedigree Software Revolutionizes Medical Genetics Department](/content/casestudies/case-study-addenbrookes/index.html): PhenoTips' pedigree software revolutionised Addenbrookes' medical genetics department. A case study on Cambridge University Hospitals NHS Foundation Trust. (2,062 words) - [Pedigree Update: Enhanced Gender and Sex Representation](/content/blog/gender-pedigree-update/index.html): A new update to PhenoTips' pedigree maker supports inclusive genetic counseling practice with customized symbols and separate fields for sex and gender. (1,762 words) - [privacy-policy/index.html](/content/privacy-policy/index.html) (1 words) - [speaker-series/index.html](/content/speaker-series/index.html) (1 words) - [team/index.html](/content/team/index.html) (1 words) - [PhenoTips and DNAstack Partner to Deliver Sovereign Genomic Medicine Platform for Canadian Health Systems](/content/press/index.html): Read the latest news on PhenoTips, PhenoTips' partnerships, and the Genomic Health Record, from new clients, to research projects, to award announcements. (1,889 words) - [Challenging the status quo of genomic medicine.](/content/our-story/index.html): Challenging the status quo of genomic medicine, we are dedicated to providing you with software that brings your workflow into the modern age of genomics. (2,107 words) - [National Data Opt-Out Statement](/content/data-opt-out/index.html): All press National Data Opt-Out Statement Gene42 Inc. o/a PhenoTips Purpose The National Data Opt-Out (NDO) is an NHS England policy that allows patients in England to opt out of their confidential patient information (CPI) being used for purposes beyond their individual care and treatment, such as research and planning. This statement sets out PhenoTips’ (1,644 words) - [2025: PhenoTips’ Year in Review](/content/blog/index.html) (1,275 words) - [See the complete Genomic Health Record in action.](/content/book-a-demo/index.html): Send us a message Unsure if PhenoTips is the right fit for your team? Request additional information. Send a Message The information you provide will be used in accordancewith the terms of the PhenoTips privacy policy. Schedule a demo Book a 30-minute, one-on-one meeting to see if PhenoTips is the right fit for your team. (1,421 words) - [Do not sell my data - PhenoTips](/content/do-not-sell/index.html): Gene42 does not sell personal information and does not share personal information for cross-context behavioral advertising as those terms are defined under the CCPA/CPRA.Gene42's third-party processors (HubSpot) operate as service providers under written DPAs that prohibit the secondary use of personal information.For more information on your rights (right to know, access, delete, correct, limit sensitive (1,416 words) - [Case Studies](/content/casestudies/index.html): Case Studies Hear from our clients, read the stories behind the software. (1,466 words) - [PHENOTIPS ENTERPRISE FEATURE](/content/cancer-risk-assessment/index.html): Simplify your cancer risk assessment for breast and ovarian cancer, multiple genes, and non-cancer conditions to one click, launched within pedigrees. (1,775 words) - [PHENOTIPS ENTERPRISE FEATURE](/content/seamless-integrations/index.html): PHENOTIPS ENTERPRISE FEATURE Seamless Integrations Empower seamless, quality care. Unite your systems with a single sign-on by integrating your Genomic Health Record with any Electronic Medical Record, Laboratory Information Management System, Variant Prioritization tool, or Matchmaking system, regardless of the make or model. Book a demo SECURITY AND GOVERNANCE Secure your workflow Genetic information is (1,674 words) - [PHENOTIPS ENTERPRISE FEATURE](/content/patient-questionnaire/index.html): PHENOTIPS ENTERPRISE FEATURE Pre-Visit Patient Questionnaire Send your patients a digital pre-visit questionnaire that automatically draws their pedigree before they arrive, leaving you free to focus on your patient instead of their paperwork Book a demo See the Pre-Visit Patient Questionnaire in action From scheduling to automated family trees. Watch the 3-minute video walkthrough of (1,353 words) - [RESEARCH TEAM](/content/pricing/index.html): A Genomic Health Record for your unique needs Whether you’re a research team or a representative of a clinic or hospital, there is a PhenoTips solution that will power your genomic workflow. RESEARCH TEAM $ 399 /mo includes 5 users, then $25/user Bring the power of structured data to your team’s workflow PhenoTips Core Suite (1,595 words) - [We'd like to hear from you.](/content/contact/index.html): Get in touch. EMAIL US hello@phenotips.com We'd like to hear from you. If you have a question or would like to reach out about any of our solutions, please get in touch. (1,374 words) - [PHENOTIPS CORE FEATURE](/content/phenotips-pedigree-maker-tool/index.html): Every PhenoTips Genomic Health Record comes equipped with an intuitive and inclusive pedigree chart maker capable of capturing complex family history (1,819 words) - [PHENOTIPS FOR health systems](/content/health-systems/index.html): PhenoTips is a proud partner of the NHS, helping trusts and regional alliances collaborate, engage patients, and offer consistent, accessible genomic care. (2,110 words) - [PHENOTIPS core feature](/content/structured-patient-data-and-clinical-insights/index.html): Centralize genomic care and bring insights into the digital age with patient records make patient information AI-ready, standardized, searchable, and shareable. (1,713 words) - [PHENOTIPS FOR health systems](/content/rare-disease/index.html): With deep phenotyping, diagnostic insights, searchable records and seamless collaboration, PhenoTips enhances care and diagnosis for even the rarest conditions. (1,407 words) - [PHENOTIPS FOR Cancer genetics](/content/cancer-genetics/index.html): Simplify patient care with PhenoTips' complete Genomic Health Record for cancer genetics: pedigree maker, pedigree-embedded cancer risk assessment, and more. (1,666 words) - [The Core Genomic Health Record](/content/core-genomic-health-record/index.html): Our core software is a searchable database of patient records linked to family records, complete with a pedigree maker & the tools needed to digitize genomics. (1,424 words) ## Resources - [Full Page Index](/index.html): Browse all cached pages with rich metadata - [About This Cache](/content/about.html): Methodology, technical details, and usage guidelines - [XML Sitemap](/sitemap.xml): Machine-readable sitemap for crawler discovery - [Robots.txt](/robots.txt): Crawler directives