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Meier-Gorlin syndrome 6
Summary
- Definition
- A Meier-Gorlin syndrome that has_material_basis_in heterozygous mutation in the GMNN gene on chromosome 6p22.
- Super Class
- Meier-Gorlin syndrome autosomal dominant disease
External Links
- Disease Ontology
- DOID:0080517
- Mondo Disease Ontology
- OMIM
