nephrotic syndrome type 26

Term ID

DOID:0061193

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. https://pubmed.ncbi.nlm.nih.gov/35419533/

References

• MIM:620049

Ontology

Human Disease   ( DOID:0061193 )