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

• OMIM:617729

Ontology

Human Disease   ( DOID:0080245 )