Term Name:	nephrotic syndrome type 26
Synonyms:	NPHS26
Definition:	A familial nephrotic syndrome characterized by onset of proteinuria in the first months or years of life that has_material_basis_in homozygous or compound heterozygous mutation in the LAMA5 gene on chromosome 20q13.
Ontology:	Human Disease [DOID:0061193]   ( DOID:0061193 )