pseudoxanthoma elasticum

Summary
Synonym
  • Gronblad-Strandberg syndrome
Definition
A connective tissue disease that is characterized by the accumulation of deposits of calcium and other minerals in elastic fibers, which are a component of connective tissue, this can result in changes in the skin, eyes, cardiovascular system and gastrointestinal system.
Super Class
autosomal recessive disease connective tissue disease
Disease Ontology
DOID:2738
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying all 10 entries
Gene ID Gene Symbol Description Source
368 ABCC6 ATP binding cassette subfamily C member 6
847 CAT catalase
2006 ELN elastin
2876 GPX1 glutathione peroxidase 1
4313 MMP2 matrix metallopeptidase 2
5167 ENPP1 ectonucleotide pyrophosphatase/phosphodiesterase 1
6648 SOD2 superoxide dismutase 2
7422 VEGFA vascular endothelial growth factor A
64131 XYLT1 xylosyltransferase 1
64132 XYLT2 xylosyltransferase 2
Displaying all 8 entries
Gene ID Gene Symbol Description Source
14775 Gpx1 glutathione peroxidase 1
17390 Mmp2 matrix metallopeptidase 2
18605 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1
20656 Sod2 superoxide dismutase 2, mitochondrial
22339 Vegfa vascular endothelial growth factor A
27421 Abcc6 ATP-binding cassette, sub-family C member 6
217119 Xylt2 xylosyltransferase II
233781 Xylt1 xylosyltransferase 1
Displaying all 7 entries
Gene ID Gene Symbol Description Source
24787 Sod2 superoxide dismutase 2
64133 Xylt1 xylosyltransferase 1
64134 Xylt2 xylosyltransferase 2
81642 Abcc6 ATP binding cassette subfamily C member 6
81686 Mmp2 matrix metallopeptidase 2
83785 Vegfa vascular endothelial growth factor A
85496 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
38288 oxt peptide O-xylosyltransferase
Displaying all 3 entries
Gene ID Gene Symbol Description Source
30682 vegfaa vascular endothelial growth factor Aa
560951 xylt1 xylosyltransferase I
563446 xylt2 xylosyltransferase II
Displaying all 5 entries
Gene ID Gene Symbol Description Source Organism
444363 xylt1.L xylosyltransferase I L homeolog Xenopus laevis (African clawed frog)
448400 xylt2 xylosyltransferase II Xenopus tropicalis (tropical clawed frog)
100145490 xylt1 xylosyltransferase I Xenopus tropicalis (tropical clawed frog)
108701100 xylt2.L xylosyltransferase II L homeolog Xenopus laevis (African clawed frog)
108703114 xylt1.S xylosyltransferase I S homeolog Xenopus laevis (African clawed frog)
Displaying all 7 entries
Gene ID Gene Symbol Description Source
179665 C27A7.3 Ectonucleotide pyrophosphatase/phosphodiesterase C27A7.1;Ectonucleotide pyrophosphatase/phosphodiesterase C27A7.3
179991 zmp-4 Hemopexin;Peptidase metallopeptidase domain-containing protein
180351 W01F3.2 Uncharacterized protein
180409 mrp-1 Multidrug resistance-associated protein 1
181178 gpx-5 Glutathione peroxidase
182513 gpx-3 Glutathione peroxidase 3
190099 sqv-6 Xylosyltransferase sqv-6;protein xylosyltransferase
Displaying all 3 entries
Gene ID Gene Symbol Description Source
850391 NPP1 nucleotide diphosphatase/phosphodiesterase NPP1
850645 BPT1 ATP-binding cassette bilirubin transporter BPT1
856699 NPP2 nucleotide diphosphatase/phosphodiesterase NPP2
The Human Phenotype Ontology
Displaying entries 1 - 10 of 55 in total
HPO ID HPO Term
HP:0000121 Nephrocalcinosis
HP:0000218 High palate
HP:0000474 Thickened nuchal skin fold
HP:0000488 Retinopathy
HP:0000505 Visual impairment
HP:0000545 Myopia
HP:0000573 Retinal hemorrhage
HP:0000592 Blue sclerae
HP:0000765 Abnormal thorax morphology
HP:0000821 Hypothyroidism
Displaying all 3 entries
Gene ID Gene Symbol Description
5167 ENPP1 ectonucleotide pyrophosphatase/phosphodiesterase 1
64131 XYLT1 xylosyltransferase 1
64132 XYLT2 xylosyltransferase 2

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Last updated: December 9, 2024