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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Larsen-like syndrome B3GAT3 type
Summary
- Synonym
-
- Larsen-like syndrome, B3GAT3 type
- multiple joint dislocations-short stature-craniofacial dysmorphism-congenital heart defects syndrome
- Definition
- A syndrome that is characterized by laxity, dislocations and contractures of the joints, short stature, foot deformities (e.g. clubfeet), broad tips of fingers and toes, short neck, dysmorphic facial features (hypertelorism, downslanting palpebral fissures, upturned nose with anteverted nares, high arched palate) and various cardiac malformations and has_material_basis_in homozygous mutation in the B3GAT3 gene on chromosome 11q12.
- Super Class
- autosomal recessive disease syndrome
External Links
- Disease Ontology
- DOID:0080575
- Mondo Disease Ontology
- ORDO
- OMIM
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| O94766 | Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 3 | |
| Q7LGC8 | Carbohydrate sulfotransferase 3 | |
| Q9UBV7 | Beta-1,4-galactosyltransferase 7 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000023 | Inguinal hernia |
| HP:0000160 | Narrow mouth |
| HP:0000175 | Cleft palate |
| HP:0000238 | Hydrocephalus |
| HP:0000248 | Brachycephaly |
| HP:0000274 | Small face |
| HP:0000308 | Microretrognathia |
| HP:0000316 | Hypertelorism |
| HP:0000337 | Broad forehead |
