OBO ID: DOID:0060364 |
Term Name: | Galloway-Mowat syndrome 1 | Search Ontology: | |
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Synonyms: |
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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 ) |
OTHER Galloway-Mowat syndrome 1 PAGES
ZEBRAFISH MODELS
Fish | Conditions | Citations |
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WT + MO1-nup133 | standard conditions | Fujita et al., 2018 |
PHENOTYPE
No data available
CITATIONS (4)
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