Ehlers-Danlos syndrome spondylodysplastic type 2

Summary
Synonym
  • EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 2
  • Ehlers-Danlos syndrome progeroid type
Definition
An Ehlers-Danlos syndrome that is characterized by aged appearance, developmental delay, short stature, craniofacial disproportion, generalized osteopenia, defective wound healing, hypermobile joints, hypotonic muscles, and loose but elastic skin and has_material_basis_in compound heterozygous mutation in the B3GALT6 gene.
Super Class
Ehlers-Danlos syndrome autosomal recessive disease
Disease Ontology
DOID:0050802
UMLS
ORDO
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
126792 B3GALT6 beta-1,3-galactosyltransferase 6
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
Q96L58 Beta-1,3-galactosyltransferase 6
The Human Phenotype Ontology
Displaying entries 1 - 10 of 100 in total
HPO ID HPO Term
HP:0000218 High palate
HP:0000238 Hydrocephalus
HP:0000343 Long philtrum
HP:0000347 Micrognathia
HP:0000358 Posteriorly rotated ears
HP:0000369 Low-set ears
HP:0000410 Mixed hearing impairment
HP:0000463 Anteverted nares
HP:0000473 Torticollis
HP:0000482 Microcornea
Displaying 1 entry
Gene ID Gene Symbol Description
126792 B3GALT6 beta-1,3-galactosyltransferase 6

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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: April 7, 2025