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Noonan syndrome 6
Summary
- Synonym
-
- NS6
- Definition
- A Noonan syndrome that has_material_basis_in heterozygous mutation in the NRAS gene on chromosome 1p13.
- Super Class
- Noonan syndrome autosomal dominant disease
External Links
- Disease Ontology
- DOID:0060584
- Mondo Disease Ontology
- MeSH
- OMIM
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 1634 | DCN | decorin | |
| 2348 | FOLR1 | folate receptor alpha | |
| 2597 | GAPDH | glyceraldehyde-3-phosphate dehydrogenase | |
| 2653 | GCSH | glycine cleavage system protein H | |
| 2720 | GLB1 | galactosidase beta 1 | |
| 2731 | GLDC | glycine decarboxylase | |
| 2821 | GPI | glucose-6-phosphate isomerase | |
| 3339 | HSPG2 | heparan sulfate proteoglycan 2 | |
| 4968 | OGG1 | 8-oxoguanine DNA glycosylase | |
| 5224 | PGAM2 | phosphoglycerate mutase 2 |
Related Glycoprotein
