|OBO ID: DOID:0080386|
|Term Name:||nephrotic syndrome type 10||Search Ontology:|
|Definition:||A familial nephrotic syndrome characterized by early childhood onset that has_material_basis_in homozygous or compound heterozygous mutation in the EMP2 gene on chromosome 16p13. https://www.ncbi.nlm.nih.gov/pubmed/24814193|
|Ontology:||Human Disease (DOID:0080386)|
|is a type of:||
OTHER nephrotic syndrome type 10 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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