sialuria

Summary
Definition
A lysosomal storage disease characterized by increased sialic acid in the urine.
Super Class
lysosomal storage disease
External Links
Disease Ontology
DOID:3659
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying all 10 entries
Gene ID Gene Symbol Description Source
1048 CEACAM5 CEA cell adhesion molecule 5
1118 CHIT1 chitinase 1
5290 PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha
5291 PIK3CB phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta
5293 PIK3CD phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta
5294 PIK3CG phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma
5973 RENBP renin binding protein
10020 GNE glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
26503 SLC17A5 solute carrier family 17 member 5
27306 HPGDS hematopoietic prostaglandin D synthase
Displaying 1 entry
Gene ID Gene Symbol Description Source
50798 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
Displaying 1 entry
Gene ID Gene Symbol Description Source
114711 Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
The Human Phenotype Ontology
Displaying entries 21 - 30 of 69 in total
HPO ID HPO Term
HP:0000319 Smooth philtrum
HP:0003645 Prolonged partial thromboplastin time
HP:0001263 Global developmental delay
HP:0008443 Neuropathic spinal arthropathy
HP:0001609 Hoarse voice
HP:0000943 Dysostosis multiplex
HP:0002574 Episodic abdominal pain
HP:0011220 Prominent forehead
HP:0001382 Joint hypermobility
HP:0007018 Attention deficit hyperactivity disorder
Displaying all 2 entries
Gene ID Gene Symbol Description
10020 GNE glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
26503 SLC17A5 solute carrier family 17 member 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: August 19, 2024