X-linked nephrolithiasis type I

Summary
Synonym
  • NPHL1
  • X-linked nephrolithiasis with renal failure
  • X-linked recessive urolithiasis type 1
  • XRN
  • nephrolithiasis 1
  • nephrolithiasis X-linked recessive type 1
Definition
A renal tubular transport disease characterized by proximal renal tubular reabsorptive failure, hypercalciuria, nephrolithiasis, and renal insufficiency with absence of rickets that has_material_basis_in hemizygous or homozygous mutation in the CLCN5 gene on chromosome Xp11.23.
Super Class
X-linked recessive disease renal tubular transport disease
Disease Ontology
DOID:0111798
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
1184 CLCN5 chloride voltage-gated channel 5
Displaying 1 entry
Gene ID Gene Symbol Description Source
12728 Clcn5 chloride channel, voltage-sensitive 5

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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