osteochondrodysplasia

Summary
Synonym
  • Cartilage Development disorder
  • Congenital anomaly of cartilage
  • Osteochondrodysplasia syndrome
  • chondrodystrophy
  • skeletal dysplasia
Definition
A bone development disease that results_in defective development of cartilage or bone.
Super Class
bone development disease
External Links
Disease Ontology
DOID:2256
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
MGI genotype (from TogoID)
Related Genes
Displaying entries 41 - 46 of 46 in total
Gene ID Gene Symbol Description Source
54187 NANS N-acetylneuraminate synthase
64131 XYLT1 xylosyltransferase 1
79158 GNPTAB N-acetylglucosamine-1-phosphate transferase subunits alpha and beta
79796 ALG9 ALG9 alpha-1,2-mannosyltransferase
84572 GNPTG N-acetylglucosamine-1-phosphate transferase subunit gamma
100507436 MICA MHC class I polypeptide-related sequence A
Displaying 1 entry
Gene ID Gene Symbol Description Source
53374 Chst3 carbohydrate sulfotransferase 3
Displaying 1 entry
Gene ID Gene Symbol Description Source
84468 Chst3 carbohydrate sulfotransferase 3
Displaying all 3 entries
Gene ID Gene Symbol Description Source
33913 CG9550 uncharacterized protein
33941 Tsp Thrombospondin
45320 trol terribly reduced optic lobes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
556800 chst3b carbohydrate (chondroitin 6) sulfotransferase 3b
559721 chst3a carbohydrate (chondroitin 6) sulfotransferase 3a
Displaying all 3 entries
Gene ID Gene Symbol Description Source Organism
100492673 chst3 carbohydrate (chondroitin 6) sulfotransferase 3 Xenopus tropicalis (tropical clawed frog)
108696269 chst3.L carbohydrate (chondroitin 6) sulfotransferase 3 L homeolog Xenopus laevis (African clawed frog)
108697511 chst3.S carbohydrate (chondroitin 6) sulfotransferase 3 S homeolog Xenopus laevis (African clawed frog)

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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