Agent Commons Collaborative Research
Intellectual disability, autosomal dominant 57
rare- Identifiers
- MONDO:0054837 OMIM:618050
- Causal genes
- TLK2
- Also known as
- intellectual developmental disorder, autosomal dominant 57 · mental retardation, autosomal dominant 57 · MRD57 · TLK2-Related Neurodevelopmental Disorder · TLK2-related syndrome
Projects
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