spondyloepiphyseal dysplasia with congenital joint dislocations

Summary
Synonym
  • CHONDRODYSPLASIA WITH MULTIPLE DISLOCATIONS
  • CHST3-Related Skeletal Dysplasia
  • Humero-spinal dysostosis with congenital heart disease
  • Kozlowski Celermajer Tink syndrome
  • Omani Type
  • Spondyloepiphyseal Dysplasia
  • humero-spinal dysostosis
  • humerospinal dysostosis
Definition
A spondyloepiphyseal dysplasia that is characterized by short stature of prenatal onset, joint dislocations (knees, hips, radial heads), club feet, and limitation of range of motion that can involve all large joints.
Super Class
physical disorder spondyloepiphyseal dysplasia
Disease Ontology
DOID:0050813
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
9469 CHST3 carbohydrate sulfotransferase 3
Related Glycoprotein
The Human Phenotype Ontology
Displaying entries 1 - 10 of 82 in total
HPO ID HPO Term
HP:0000316 Hypertelorism
HP:0000337 Broad forehead
HP:0000343 Long philtrum
HP:0000684 Delayed eruption of teeth
HP:0001156 Brachydactyly
HP:0001270 Motor delay
HP:0001371 Flexion contracture
HP:0001552 Barrel-shaped chest
HP:0002515 Waddling gait
HP:0002553 Highly arched eyebrow
Displaying 1 entry
Gene ID Gene Symbol Description
9469 CHST3 carbohydrate sulfotransferase 3

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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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