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
Subtypes
| Disease | Subtypes | ||
|---|---|---|---|
| No rare subtypes. | |||
Projects
Including projects on subtypes.
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