Search Ontology:
Human Disease
Galloway-Mowat syndrome 7
- Term ID
- DOID:0061290
- Synonyms
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- Definition
- A Galloway-Mowat syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the NUP107 gene on chromosome 12q15. https://pubmed.ncbi.nlm.nih.gov/28280135/
- References
- Ontology
- Human Disease ( DOID:0061290 )
Other Pages
Genes Involved
Zebrafish Models