HNRNP-Related Disorders
A family of rare genetic neurodevelopmental disorders caused by variants in HNRNP genes. Each condition has unique features, but they share common mechanisms that connect our research and community.
All HNRNP Disorders
Click on any disorder to learn about its specific clinical features, current research, and connect with other families in the community.
HNRNPC-RNDD
HNRNPCAutosomal DominantHNRNPC-Related Neurodevelopmental Disorder
PTBP1-RNDD
PTBP1Autosomal DominantPTBP1 (HNRNPI)-Related Neurodevelopmental Disorder
HNRNPG-RNDD
RBMXX-LinkedHNRNRPG (RBMX)-Related Neurodevelopmental Disorders
HNRNPH1-RNDD
HNRNPH1Autosomal DominantHNRNPH1-Related Neurodevelopmental Disorder
HNRNPH2-RNDD
HNRNPH2X-LinkedHNRNPH2-Related Neurodevelopmental Disorder
Au-Kline Syndrome
HNRNPKAutosomal DominantHNRNPK-Related Neurodevelopmental Disorder (Au-Kline Syndrome)
HNRNPR-RNDD
HNRNPRAutosomal DominantHNRNPR-Related Neurodevelopmental Disorder
HNRNPU-RNDD
HNRNPUAutosomal DominantHNRNPU-Related Neurodevelopmental Disorder
SYNCRIP-RNDD
SYNCRIPAutosomal DominantSYNCRIP/HNRNPQ-Related Neurodevelopmental Disorder
What's Next?
Explore more resources to understand HNRNP disorders