| Metadata | |
|---|---|
| ID | DOID:0060364 |
| Name | Galloway-Mowat syndrome 1 |
| Definition | A Galloway-Mowat syndrome that has_material_basis_in homozygous mutation in the WDR73 gene on chromosome 15q25. https://en.wikipedia.org/wiki/Galloway_Mowat_syndrome, https://pubmed.ncbi.nlm.nih.gov/26123727/ |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
autosomal recessive spinocerebellar ataxia 5 [EXACT] Galloway syndrome [EXACT] microcephaly, hiatal hernia and nephrotic syndrome [EXACT] nephrosis-microcephaly syndrome [EXACT] nephrosis-neuronal dysmigration syndrome [EXACT] SCAR5 [EXACT] |
| Parent Relationships | |
| Subclass Logical Relationships |
has material basis in some autosomal recessive inheritance |