Visualize Submit Comment

Metadata
ID	DOID:0061193
Name	nephrotic syndrome type 26
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. https://pubmed.ncbi.nlm.nih.gov/35419533/
Xrefs	MIM:620049
Synonyms	NPHS26 [EXACT]
Parent Relationships	is_a familial nephrotic syndrome is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance