Hemophilia A X-linked pedigree
A hemophilia A pedigree can show an X-linked inheritance pattern across a family. Mark affected relatives, known carrier females, unaffected relatives, and the proband who prompted the assessment. Put each generation on its own line and place children below the relevant parent pair, which makes the pattern easier to discuss. This is useful for genetics education and for preparing a concise family-history summary. It does not establish a diagnosis or replace genetic counseling. Information about bleeding history, factor testing, genetic results, and family planning needs interpretation by an appropriate clinical professional. Keep sensitive health information limited to people who need it.
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Scenario
X-linked inheritance
Key decisions
- Use the X-linked mode: Match the inheritance pattern to the pedigree.
- Mark carrier females: Distinguish known carrier status.
- Show affected males: Keep the pattern visible across generations.
- Identify the proband: Mark the family member being assessed.
When to reuse this
Use this as a teaching diagram for an X-linked family history; clinical interpretation needs qualified review.
Frequently asked questions
What does an X-linked pedigree show?
How are carrier females shown?
Can a pedigree diagnose hemophilia A?
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