|OBO ID: DOID:0080389|
|Term Name:||nephrotic syndrome type 8||Search Ontology:|
|Definition:||A familial nephrotic syndrome characterized by neonatal or early childhood onset steroid resistant renal disease that has_material_basis_in homozygous or compound heterozygous mutation in the ARHGDIA gene on chromosome 17q25. (2)|
|Ontology:||Human Disease (DOID:0080389)|
|is a type of:||
OTHER nephrotic syndrome type 8 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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