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Ehlers-Danlos syndrome spondylodysplastic type 1
Summary
- Definition
- An Ehlers-Danlos syndrome that is characterized by short stature, developmental anomalies of the forearm bones and elbow, and bowing of extremities, in addition to the classic stigmata of Ehlers-Danlos syndrome, including joint laxity, skin hyperextensibility, and poor wound healing and that has_material_basis_in homozygous or compound heterozygous mutation in the B4GALT7 gene on chromosome 5q35.
- Super Class
- Ehlers-Danlos syndrome autosomal recessive disease
External Links
- Disease Ontology
- DOID:0080738
- Mondo Disease Ontology
- OMIM
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 42991 | beta4GalT7 | beta-4-galactosyltransferase 7 |
| Gene ID | Gene Symbol | Description | Source | Organism |
|---|---|---|---|---|
| 495369 | b4galt7.S | xylosylprotein beta 1,4-galactosyltransferase, polypeptide 7 S homeolog | Xenopus laevis (African clawed frog) | |
| 100144979 | b4galt7 | xylosylprotein beta 1,4-galactosyltransferase, polypeptide 7 | Xenopus tropicalis (tropical clawed frog) | |
| 108710989 | b4galt7.L | xylosylprotein beta 1,4-galactosyltransferase, polypeptide 7 L homeolog | Xenopus laevis (African clawed frog) |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9UBV7 | Beta-1,4-galactosyltransferase 7 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000316 | Hypertelorism |
| HP:0000337 | Broad forehead |
| HP:0000347 | Micrognathia |
| HP:0000369 | Low-set ears |
| HP:0000387 | Absent earlobe |
| HP:0000520 | Proptosis |
| HP:0000540 | Hypermetropia |
| HP:0000592 | Blue sclerae |
| HP:0000768 | Pectus carinatum |
| HP:0000774 | Narrow chest |
