Visualize Submit Comment
Metadata
ID DOID:0080247
Name Galloway-Mowat syndrome 5
Definition A Galloway-Mowat syndrome that has_material_basis_in homozygous mutation in the TPRKB gene on chromosome 2p13.
https://pubmed.ncbi.nlm.nih.gov/28805828/
Xrefs

OMIM:617731

Parent Relationships

is_a Galloway-Mowat syndrome

Add an item to the term tracker