Huntington disease pedigree.
This simple pedigree shows an autosomal dominant pattern using Huntington disease as the clinical example. An affected parent has an affected child in the next generation, while unaffected relatives are also shown so the family structure is easy to read. The affected granddaughter is the proband, the person whose history brought the family to clinical attention. This is the kind of compact drawing used early in a consultation or in genetics teaching, before dates, test reports and additional relatives are added. A pedigree shows reported family history and relationships; it cannot determine whether a person has inherited a variant. Genetic testing and medical decisions should be discussed with a qualified clinician or counselor.
Open it in the AI editor with a prompt pre-filled — keep what works, change what doesn't.
Scenario
Genetic counseling
Key decisions
- Successive generations: Affected relatives appear in each generation.
- Unaffected partners: Partners are shown as unaffected.
- Index case: The affected granddaughter is the proband.
When to reuse this
Use this simple chart to introduce autosomal dominant inheritance in a counseling or teaching conversation.
Frequently asked questions
What is autosomal dominant inheritance?
Why are unaffected relatives included?
What does the arrow identify?
Tweak it with chat, export PNG/SVG, or fork it for your own use case.