nephrotic syndrome type 5

Summary
Synonym
  • nephrotic syndrome type 5, with or without ocular abnormalities
Definition
A familial nephrotic syndrome characterized by prenatal or neonatal onset of progressive renal failure with proteinurea and edema that has_material_basis_in homozygous or compound heterozygous mutation in the LAMB2 gene on chromosome 3p.
Super Class
autosomal recessive disease familial nephrotic syndrome
Disease Ontology
DOID:0080380
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
3913 LAMB2 laminin subunit beta 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
16779 Lamb2 laminin, beta 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
25473 Lamb2 laminin subunit beta 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
177292 lam-1 Laminin subunit beta-1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024