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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
External Links
- Disease Ontology
- DOID:0050802
- Mondo Disease Ontology
- UMLS
- ORDO
- OMIM
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 35848 | beta3GalTII | beta-1,3-Galactosyltransferase II |
| Gene ID | Gene Symbol | Description | Source | Organism |
|---|---|---|---|---|
| 548849 | b3galt6 | Beta-1,3-galactosyltransferase 6 | Xenopus tropicalis (tropical clawed frog) | |
| 108696563 | b3galt6.L | Beta-1,3-galactosyltransferase 6 L homeolog | Xenopus laevis (African clawed frog) | |
| 108697636 | b3galt6.S | Beta-1,3-galactosyltransferase 6 S homeolog | Xenopus laevis (African clawed frog) |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P07585 | Decorin | |
| P13611 | Versican core protein | |
| P13727 | Bone marrow proteoglycan | |
| P98160 | Basement membrane-specific heparan sulfate proteoglycan core protein | |
| Q96L58 | Beta-1,3-galactosyltransferase 6 | |
| Q9UBV7 | Beta-1,4-galactosyltransferase 7 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001181 | Adducted thumb |
| HP:0001250 | Seizure |
| HP:0001252 | Hypotonia |
| HP:0001270 | Motor delay |
| HP:0001297 | Stroke |
| HP:0001319 | Neonatal hypotonia |
| HP:0001357 | Plagiocephaly |
| HP:0001363 | Craniosynostosis |
| HP:0001382 | Joint hypermobility |
| HP:0001385 | Hip dysplasia |
