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Repository for lectin-assisted multimodality data
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
diastrophic dysplasia
Summary
- Definition
- An osteochondrodysplasia that has_material_basis_in abnormal cartilage development due to mutations in the SLC26A2 gene which results_in short limb dwarfism.
- Super Class
- autosomal recessive disease osteochondrodysplasia
External Links
- Disease Ontology
- DOID:14687
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- OMIM
- GARD
- MGI genotype (from TogoID)
- WikiPathways (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P50443 | Sulfate transporter |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001609 | Hoarse voice |
| HP:0001762 | Talipes equinovarus |
| HP:0002176 | Spinal cord compression |
| HP:0002751 | Kyphoscoliosis |
| HP:0002857 | Genu valgum |
| HP:0002938 | Lumbar hyperlordosis |
| HP:0002947 | Cervical kyphosis |
| HP:0002999 | Patellar dislocation |
| HP:0003026 | Short long bone |
| HP:0003071 | Flattened epiphysis |
