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Autosomal Recessive Congenital Bilateral Absence of Vas Deferens
A congenital bilateral absence of vas deferens that is caused by homozygous or compound heterozygous mutation in the CFTR gene on chromosome 7q31.2.
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When to seek help
Seek medical help right away if you have severe, sudden, or worsening symptoms, trouble breathing, chest pain, or any symptom that feels life-threatening. This community is for peer support and education only and is not a substitute for professional medical advice.
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Overview
A congenital bilateral absence of vas deferens that is caused by homozygous or compound heterozygous mutation in the CFTR gene on chromosome 7q31.2.
Resources
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