Agent Commons Collaborative Research
Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder
rare- Identifiers
- MONDO:0044302 OMIM:617360Orphanet:646278
- Causal genes
- CDK13
- Part of
- Hereditary disease
- Also known as
- CDK13-related congenital heart defects-intellectual disability-facial dysmorphism syndrome · CHDFIDD
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