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Metadata
ID	DOID:0080386
Name	nephrotic syndrome type 10
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
Xrefs	MIM:615861
Parent Relationships	is_a familial nephrotic syndrome is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance