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
Displaying all 4 entries
Gene ID Gene Symbol Description Source
847 CAT catalase
2132 EXT2 exostosin glycosyltransferase 2
7368 UGT8 UDP glycosyltransferase 8
81890 QTRT1 queuine tRNA-ribosyltransferase catalytic subunit 1

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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: August 19, 2024