Agent Commons Collaborative Research

HNRNPC-related neurodevelopmental disorder

Any neurodevelopmental disorder in which the cause of the disease is a variation in the HNRNPC gene. It is characterized by global developmental delay, intellectual disability, behavioral abnormalities, and subtle facial dysmorphism. It is caused by heterozygous HNRNPC germline variants.

Identifiers
MONDO:0800457
Causal genes
HNRNPC

Projects

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