Genetic counselling cases, clinically defensible from referral to cascade testing.
Structured session records, an interactive pedigree builder, guided ACMG variant classification and auto-calculated Manchester risk scoring — replacing paper forms and spreadsheets with one audit-ready genetics workspace inside Odoo.
The problem
Genetic counselling teams juggle pedigrees, HGVS variant notation, ACMG classification and hereditary cancer risk scores across paper forms, generic EMR free-text notes and spreadsheets that do not connect to the hospital’s patient records. A misclassified variant carries real clinical consequences, yet the specialist data behind these decisions is scattered, unstructured and impossible to audit.
The solution
One workspace to record a counselling session, draw an interactive pedigree, classify variants with guided ACMG criteria, auto-calculate Manchester risk, and generate cascade-testing outreach to at-risk relatives — all with a full chatter audit trail and a de-identified patient portal.
Built for the genetics counselling workflow
Every capability below is implemented in the module.
Interactive pedigree builder
Draw and read a standard-notation family-tree diagram right on the session, instead of recording pedigree as flat data entry.
Guided ACMG/AMP variant classification
Select the evidence criteria that apply and get an automatic suggested classification, flagged if the counsellor’s final call diverges.
Auto-calculated Manchester risk scoring
The 10-year hereditary cancer risk score and risk band are derived live from entered factors, with BOADICEA capture alongside — no off-system arithmetic.
HGVS notation validation
Coding and protein notation are checked against the standard HGVS format as they are entered, catching malformed notation before it reaches the record.
Cascade testing & batch outreach
Generate and track cascade letters for every at-risk relative in a family in a single batch, instead of one letter at a time.
Gene & panel library with OMIM lookup
Select a pre-configured gene panel instead of re-typing genes, and open OMIM reference data for any gene without leaving the record.
External lab result import
Import results directly from a CSV file exported by the lab’s own system, eliminating manual re-keying.
Staged workflow with full audit trail
Sessions move through Draft, Confirmed and Done with tracked fields, chatter and scheduled follow-up activities for every case.
De-identified patient portal
Patients securely view a de-identified summary of their counselling outcome through the standard Odoo portal.
How it works
Open a session
Record the patient, referral indication and the gene panel or genes requested.
Draw, score and classify
Build the pedigree, enter Manchester risk factors and classify each variant against ACMG criteria.
Review and confirm
The counsellor and attending doctor review findings in the chatter and move the session to Confirmed or Done.
Notify and track
Batch-generate cascade letters for at-risk relatives and share a de-identified summary to the patient portal.
Frequently asked
No sales fog. If your question isn't here, email us and we'll answer it the same way.
No. The patient is a standard Odoo contact and the admission reference is an optional free-text field, so standalone genetics clinics can adopt the app without any third-party hospital suite.
Buy it on the Odoo App Store
Purchase, download and install directly from the official Odoo Apps Store — you'll always get the latest supported build.
Genetic Counselling Clinic
An interactive pedigree builder, guided ACMG/AMP classification, HGVS validation and auto-calculated Manchester scoring — with cascade testing outreach and lab result import.
Buy on Odoo App Store