| Term Name: | Galloway-Mowat syndrome 10 |
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| Synonyms: | |
| Definition: | A Galloway-Mowat syndrome characterized by onset of symptoms soon after birth that has_material_basis_in homozygous or compound heterozygous mutation in the YRDC gene on chromosome 1p34. |
| Ontology: | Human Disease [DOID:0061293] ( DOID:0061293 ) |