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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
obsolete Matthew-Wood syndrome
Summary
- Definition
- A syndrome that is characterized by microphthalmia or anophthalmia, pulmonary agenesis, and diaphragmatic defect.
External Links
- Disease Ontology
- DOID:0050819
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 2215 | FCGR3B | Fc gamma receptor IIIb | |
| 2220 | FCN2 | ficolin 2 | |
| 2224 | FDPS | farnesyl diphosphate synthase | |
| 2262 | GPC5 | glypican 5 | |
| 2525 | FUT3 | fucosyltransferase 3 (Lewis blood group) | |
| 2526 | FUT4 | fucosyltransferase 4 | |
| 2571 | GAD1 | glutamate decarboxylase 1 | |
| 2591 | GALNT3 | polypeptide N-acetylgalactosaminyltransferase 3 | |
| 2597 | GAPDH | glyceraldehyde-3-phosphate dehydrogenase | |
| 2752 | GLUL | glutamate-ammonia ligase |
Related Glycoprotein
