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
Disease Ontology
DOID:0060285
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
60529 ALX4 ALX homeobox 4

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024