|OBO ID: DOID:0080392|
|Term Name:||nephrotic syndrome type 17||Search Ontology:|
|Definition:||A familial nephrotic syndrome that has_material_basis_in by homozygous or compound heterozygous mutation in the NUP85 gene on chromosome 17q25. https://www.ncbi.nlm.nih.gov/pubmed/30179222|
|Ontology:||Human Disease (DOID:0080392)|
|is a type of:||
OTHER nephrotic syndrome type 17 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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