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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
spina bifida
Summary
- Definition
- A neural tube defect that is characterized by incomplete closing of the spine and membranes around the spinal cord during early development.
- Super Class
- neural tube defect
External Links
- Disease Ontology
- DOID:0080016
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- GARD
- MGI genotype (from TogoID)
- WikiPathways (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 28 | ABO | ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase | |
| 328 | APEX1 | apurinic/apyrimidinic endodeoxyribonuclease 1 | |
| 410 | ARSA | arylsulfatase A | |
| 952 | CD38 | CD38 molecule | |
| 1119 | CHKA | choline kinase alpha | |
| 1312 | COMT | catechol-O-methyltransferase | |
| 2262 | GPC5 | glypican 5 | |
| 2348 | FOLR1 | folate receptor alpha | |
| 2350 | FOLR2 | folate receptor beta | |
| 3098 | HK1 | hexokinase 1 |
Related Glycoprotein
