asked 130k views
1 vote
A child is diagnosed with a rare genetic disease. Neither parent has the disease. How might the child have inherited the disorder?

1 Answer

7 votes

Answer:

Recessive genes.

Step-by-step explanation:

Both parents were likely carriers of the rare disease, but dominant traits allowed them not to be affected by it.

answered
User Madusanka
by
7.6k points

No related questions found

Welcome to Qamnty — a place to ask, share, and grow together. Join our community and get real answers from real people.