Search Ontology:
Human Disease
Galloway-Mowat syndrome 1
- Term ID
- DOID:0060364
- Synonyms
-
- autosomal recessive spinocerebellar ataxia 5
- Galloway syndrome
- microcephaly, hiatal hernia and nephrotic syndrome
- Definition
- A Galloway-Mowat syndrome that has_material_basis_in homozygous mutation in the WDR73 gene on chromosome 15q25. (2)
- References
- Ontology
- Human Disease ( DOID:0060364 )
- is a type of
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Genes Involved
| Human Gene | Zebrafish Ortholog | OMIM Term | Disease | OMIM Phenotype ID |
|---|---|---|---|---|
| WDR73 | Galloway-Mowat syndrome 1 | Galloway-Mowat syndrome 1 | 251300 |
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Zebrafish Models
| Fish | Conditions | Disease | Citation |
|---|---|---|---|
| WT + MO1-nup133 | standard conditions | Galloway-Mowat syndrome 1 | Fujita et al., 2018 |
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