| Term Name: | Galloway-Mowat syndrome 6 |
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| Synonyms: | |
| Definition: | A Galloway-Mowat syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the WDR4 gene on chromosome 21q22. |
| Ontology: | Human Disease [DOID:0061289] ( DOID:0061289 ) |