Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
parietal foramina
Summary
- Synonym
-
- Caitlin marks
- enlarged parietal foramina
- hereditary cranium bifidum
- Definition
- An inherited neural tube defect that is characterized by enlarged openings in the parietal bones of the skull, has_material_basis_in mutation in the ALX4 gene or MSX2 gene.
- Super Class
- neural tube defect
External Links
- Disease Ontology
- DOID:0060285
- Mondo Disease Ontology
- MeSH
- UMLS
- ORDO
- OMIM
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P04040 | Catalase | |
| Q16880 | 2-hydroxyacylsphingosine 1-beta-galactosyltransferase | |
| Q93063 | Exostosin-2 | |
| Q9BXR0 | Queuine tRNA-ribosyltransferase catalytic subunit 1 |
