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Standards Ontologies Notations
hypophosphatemic nephrolithiasis/osteoporosis 1

Summary
Definition
A hypophosphatemic nephrolithiasis/osteoporosis that has_material_basis_in heterozygous mutation in the SLC34A1 gene on chromosome 5q35.
Super Class
autosomal dominant disease hypophosphatemic nephrolithiasis/osteoporosis
External Links
Disease Ontology
DOID:0080077
Mondo Disease Ontology
MeSH
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
6569 SLC34A1 solute carrier family 34 member 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
20505 Slc34a1 solute carrier family 34 (sodium phosphate), member 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
25548 Slc34a1 solute carrier family 34 member 1
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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

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Last updated: August 19, 2024