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Human Disease

Galloway-Mowat syndrome 3

Term ID
DOID:0080245
Synonyms
Definition
A Galloway-Mowat syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the OSGEP gene on chromosome 14q11. https://pubmed.ncbi.nlm.nih.gov/28805828/
References
Ontology
Human Disease   ( DOID:0080245 )
Relationships
is a type of
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Genes Involved
Zebrafish Models