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Standards Ontologies Notations
familial nephrotic syndrome

Summary
Synonym
  • Congenital nephrotic syndrome
Definition
A nephrotic syndrome that has_material_basis_in genetic mutations.
Super Class
monogenic disease nephrotic syndrome
Disease Ontology
DOID:2590
MeSH
UMLS
NCI Thesaurus
OMIM
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
3911 LAMA5 laminin subunit alpha 5
23500 DAAM2 dishevelled associated activator of morphogenesis 2
Displaying all 2 entries
Gene ID Gene Symbol Description Source
16776 Lama5 laminin, alpha 5
76441 Daam2 dishevelled associated activator of morphogenesis 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
140433 Lama5 laminin subunit alpha 5
Displaying 1 entry
Gene ID Gene Symbol Description Source
38723 LanA Laminin A
Displaying 1 entry
Gene ID Gene Symbol Description Source
177956 epi-1 Laminin-like protein epi-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