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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 |
|---|---|---|---|
| 57016 | AKR1B10 | aldo-keto reductase family 1 member B10 | |
| 57104 | PNPLA2 | patatin like phospholipase domain containing 2 | |
| 57126 | CD177 | CD177 molecule | |
| 57214 | CEMIP | cell migration inducing hyaluronidase 1 | |
| 64083 | GOLPH3 | golgi phosphoprotein 3 | |
| 64781 | CERK | ceramide kinase | |
| 79679 | VTCN1 | V-set domain containing T cell activation inhibitor 1 | |
| 113026 | PLCD3 | phospholipase C delta 3 | |
| 130120 | REG3G | regenerating family member 3 gamma | |
| 347527 | ARSH | arylsulfatase family member H |
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 |
