|OBO ID: DOID:0080385|
|Term Name:||nephrotic syndrome type 11||Search Ontology:|
|Definition:||A familial nephrotic syndrome characterized by onset in the first decade of life of steroid resistant progressive renal disease that has_material_basis_in homozygous or compound heterozygous mutation in the NUP107 gene on chromosome 12q15. https://www.ncbi.nlm.nih.gov/pubmed/26411495|
|Ontology:||Human Disease (DOID:0080385)|
|is a type of:||
OTHER nephrotic syndrome type 11 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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