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Kleefstra syndrome 2
Summary
- Definition
- A Kleefstra syndrome that is characterized by delayed psychomotor development, variable intellectual disability, and mild dysmorphic features and has_material_basis_in heterozygous mutation in the KMT2C gene on chromosome 7q36.
- Super Class
- Kleefstra syndrome autosomal dominant disease
External Links
- Disease Ontology
- DOID:0080598
- Mondo Disease Ontology
- ORDO
- OMIM
- WikiPathways (from TogoID)
