Term Name: | nephrotic syndrome type 10 |
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Synonyms: | |
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. |
Ontology: | Human Disease [DOID:0080386] ( DOID:0080386 ) |