Free genogram template
Medical Genogram Template (Free, Editable)
Quick answer
Download the medical genogram template
- Blank template (PDF)US Letter, print and fill in by hand
- Editable PowerPoint (.pptx)Every symbol and line is a shape; opens in Google Slides and Keynote
- Filled example + blank (PDF)Two pages: the example with its key, then the blank
- High-resolution example (PNG)2400 px wide, free to reuse with credit
- Vector blank (SVG)Edit in Illustrator, Inkscape, Figma or Canva
When to use a medical genogram template
Use this template to take a family health history: a primary care intake, a pre-appointment form for genetics or oncology, or a medical student's family history assignment. It records the biological relatives that matter for risk (parents, siblings, children, grandparents, aunts and uncles) with conditions, ages at onset and ages and causes of death.
The key uses shading inside each symbol: fill the left half for a physical or mental illness, the bottom half for alcohol or drug misuse, stripes for a suspected condition, and a quarter with a line for remission. Pick one colour per condition and write it in the colour key, so a reader can see at a glance that, for example, three relatives on the mother's side had early heart disease.
For a nursing family assessment that also covers caregiving and household, the Nursing Genogram Template fits better. For psychiatric conditions and the relationships around them, use the Mental Health Genogram Template. A medical genogram is a clinical aid; it does not replace a formal pedigree drawn by a genetics service.
The blank template and a filled-in example


Open this example in GenogramAI to start from the finished layout: it copies into your account (the Free plan holds 2 genograms) and every person, line and condition stays editable.
How to fill in a medical genogram template
- 1
Map three biological generations
Record all first-degree relatives (parents, siblings, children) and second-degree relatives (grandparents, aunts, uncles). Note ages, and age at death. - 2
Document health conditions
Shade each person for their conditions using the key, with one colour per condition. In GenogramAI, quadrants fill in the order you add conditions (top-left, top-right, bottom-left, bottom-right) and the colour key on the chart records which condition each represents; beyond four conditions the symbol switches to pie slices. - 3
Identify hereditary patterns
Write age at onset beside each condition. Look for clusters on one side of the family, early onset, and the same condition in several first-degree relatives.
Symbols this template uses
| Symbol | What it means |
|---|---|
| Left half shaded | Physical or mental illness; one colour per condition, defined in the colour key. |
| Bottom half shaded | Alcohol or drug misuse. |
| Striped shading | Suspected, undiagnosed or unconfirmed condition. |
| Quarter shaded with a line | Condition in remission, or in recovery from substance use. |
| X through the symbol | Deceased; write age and cause of death beside it. |
| Double outline | The patient (index person) whose risk you are assessing. |
Common mistakes to avoid
- Writing "cancer" without the type and the age at diagnosis, which is what determines hereditary risk.
- Mixing in step or adoptive relatives without marking them, so non-biological relatives are counted as risk.
- Using a different colour for the same condition in different people.
- Leaving deceased relatives without age and cause of death.
Who uses this template?
Primary care physicians, genetic counselors, family medicine practitioners, and medical students.
Common uses
- Family health history intake in primary care and preventive medicine
- BRCA and hereditary cancer risk assessment
- Cardiovascular disease and diabetes family pattern mapping
- Genetic counseling pre-appointment documentation
- Medical school and nursing school family history assignments
What the template covers
- Condition shading key (illness, substance misuse, suspected, remission)
- Colour-per-condition key
- Age at onset, age at death and cause of death prompts
- Family history notes area
- Online version: PNG export free; PDF and SVG export on paid plans
What is free?
Free and paid, plainly
Frequently asked questions
What is a medical genogram?
A medical genogram is a family health history diagram that maps inherited diseases, genetic conditions and health patterns across three or more generations. It uses standard symbols with shading or labels to show which relatives have which conditions, their age at onset and cause of death. It is used in primary care, genetic counseling, oncology and cardiology.
What information goes in a medical genogram?
Age or year of birth for each relative, age and cause of death for those who have died, significant diagnoses with age at onset, and any known genetic test results (for example BRCA1/2). Ancestry is also worth noting, since it changes the risk for some conditions.
How many generations should a medical genogram include?
Three generations is the usual baseline: the patient's generation, the parents' and the grandparents'. For hereditary cancer or rare conditions, a genetics service may ask for four generations or for grandparents' siblings as well; the 4 Generation Genogram Template has room for that.
Is a medical genogram the same as a pedigree chart?
They are related but differ in scope. A genetic pedigree tracks one trait or gene with standardized affected, unaffected and carrier symbols. A medical genogram captures several conditions at once, plus psychosocial context such as caregiving and relationships. Clinicians in primary care and family medicine tend to use genograms; genetics services draw pedigrees.
Should I put real patient names on a downloaded template?
A printed or locally saved template is covered by your own record-keeping rules, the same as any paper chart. The filled example on this page uses a fictional family. In GenogramAI, the Clinical plan adds zero-knowledge encryption for charts that contain patient information.
Further Reading
- McGoldrick, M., Gerson, R., & Petry, S. — Genograms: Assessment and Treatment (4th ed.). W.W. Norton & Company, 2020
- Berg, A.O. et al. — Family Health History in Clinical Practice. American Journal of Preventive Medicine, 2009
- Blazer, K.R. & Weitzel, J.N. — Genetics in Primary Care: A Faculty Development Initiative. Annals of Family Medicine, 2014