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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 |
|---|---|---|---|
| 5333 | PLCD1 | phospholipase C delta 1 | |
| 5337 | PLD1 | phospholipase D1 | |
| 5621 | PRNP | prion protein (Kanno blood group) | |
| 5728 | PTEN | phosphatase and tensin homolog | |
| 5743 | PTGS2 | prostaglandin-endoperoxide synthase 2 | |
| 5968 | REG1B | regenerating family member 1 beta | |
| 6382 | SDC1 | syndecan 1 | |
| 6383 | SDC2 | syndecan 2 | |
| 6480 | ST6GAL1 | ST6 beta-galactoside alpha-2,6-sialyltransferase 1 | |
| 6646 | SOAT1 | sterol O-acyltransferase 1 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P16444 | Dipeptidase 1 | |
| P17931 | Galectin-3 | |
| P18669 | Phosphoglycerate mutase 1 | |
| P18827 | Syndecan-1 | |
| P19320 | Vascular cell adhesion protein 1 | |
| P19367 | Hexokinase-1 | |
| P19835 | Bile salt-activated lipase | |
| P20815 | Cytochrome P450 3A5 | |
| P21217 | 3-galactosyl-N-acetylglucosaminide 4-alpha-L-fucosyltransferase FUT3 | |
| P21589 | 5'-nucleotidase |
