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
External Links
Disease Ontology
DOID:2738
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying entries 41 - 42 of 42 in total
Gene ID Gene Symbol Description Source
79158 GNPTAB N-acetylglucosamine-1-phosphate transferase subunits alpha and beta
204219 CERS3 ceramide synthase 3
Displaying all 3 entries
Gene ID Gene Symbol Description Source
18605 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1
217119 Xylt2 xylosyltransferase II
233781 Xylt1 xylosyltransferase 1
Displaying all 3 entries
Gene ID Gene Symbol Description Source
64133 Xylt1 xylosyltransferase 1
64134 Xylt2 xylosyltransferase 2
85496 Enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
38288 oxt peptide O-xylosyltransferase
Displaying all 2 entries
Gene ID Gene Symbol Description Source
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 1 entry
Gene ID Gene Symbol Description Source
190099 sqv-6 Xylosyltransferase sqv-6;protein xylosyltransferase
The Human Phenotype Ontology
Displaying entries 21 - 30 of 55 in total
HPO ID HPO Term
HP:0001382 Joint hypermobility
HP:0001482 Subcutaneous nodule
HP:0001634 Mitral valve prolapse
HP:0001645 Sudden cardiac death
HP:0001681 Angina pectoris
HP:0001723 Restrictive cardiomyopathy
HP:0001872 Abnormality of thrombocytes
HP:0002172 Postural instability
HP:0002239 Gastrointestinal hemorrhage
HP:0002514 Cerebral calcification
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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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