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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
hereditary multiple exostoses
Summary
- Synonym
-
- Multiple congenital exostosis
- Multiple exostosis syndromes
- Osteochondromatosis syndrome
- hereditary multiple exostoses 1
- hereditary multiple exostoses 2
- hereditary multiple exostoses 3
- multiple ostechondromas
- Definition
- An exostosis that has_material_basis_in a mutation on the genes EXT1, EXT2 and EXT3 which results in multiple bony spurs throughout a child's growth.
- Super Class
- autosomal dominant disease exostosis
External Links
- Disease Ontology
- DOID:206
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- ORDO
- OMIM
- MGI genotype (from TogoID)
- WikiPathways (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source | Organism |
|---|---|---|---|---|
| 398214 | ext1.L | exostosin glycosyltransferase 1 L homeolog | Xenopus laevis (African clawed frog) | |
| 399115 | ext1.S | exostosin glycosyltransferase 1 S homeolog | Xenopus laevis (African clawed frog) | |
| 448393 | ext1 | exostosin glycosyltransferase 1 | Xenopus tropicalis (tropical clawed frog) | |
| 493398 | extl3 | exostosin like glycosyltransferase 3 | Xenopus tropicalis (tropical clawed frog) | |
| 100151709 | ext2 | exostosin glycosyltransferase 2 | Xenopus tropicalis (tropical clawed frog) |
Related Glycoprotein
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0003026 | Short long bone |
| HP:0003326 | Myalgia |
| HP:0003330 | Abnormal bone structure |
| HP:0003396 | Syringomyelia |
| HP:0003406 | Peripheral nerve compression |
| HP:0003474 | Somatic sensory dysfunction |
| HP:0003959 | Deformed forearm bones |
| HP:0003977 | Deformed radius |
| HP:0004302 | Functional motor deficit |
| HP:0004322 | Short stature |
