Search Ontology:
Human Disease
Galloway-Mowat syndrome 6
- Term ID
- DOID:0061289
- Synonyms
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- Definition
- A Galloway-Mowat syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the WDR4 gene on chromosome 21q22. https://pubmed.ncbi.nlm.nih.gov/30079490/
- References
- Ontology
- Human Disease ( DOID:0061289 )
Other Pages
Genes Involved
Zebrafish Models