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Galloway-Mowat syndrome 3
Summary
- Definition
- A Galloway-Mowat syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the OSGEP gene on chromosome 14q11.
- Super Class
- Galloway-Mowat syndrome autosomal recessive disease
External Links
- Disease Ontology
- DOID:0080245
- Mondo Disease Ontology
- OMIM
